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Buying GuidesOctober 1, 2026 · 13 min read · Rongtao Medical

Aixplorer End of Service: Which Systems the 2023 Letter Covers

The 10 May 2023 Hologic letter sets an end-of-sale date, a contract-renewal cap, and a seven-year installation clock for Aixplorer 4-connector and Ultimate systems on software V7.x through V12.x—not a blanket shutdown for every scanner or a MACH replacement notice.

Buying-guide cover listing the Aixplorer end-of-sale date, the 31 October 2023 contract cap, the seven-year installation clock, and the note that MACH is not named

Which systems and software versions does the 10 May 2023 letter name?

The document is a one-page Hologic customer letter dated 10 May 2023. The title is "Product End of Life Notice & End of Service For Aixplorer 4-connector systems (Aixplorer and Aixplorer Ultimate)." The footer reference is MISC-09014_Rev002. It is signed by Massimo Rosa, Director, Ultrasound Marketing, and Christophe Pouillon, Director, Regulatory Affairs and Quality. Questions about the notice go to the address printed on the letter, breasthealth.support@hologic.com. 1

The scope sentence says: "We are writing today to inform you of the End of Life and End of Service for Aixplorer 4-connector and Aixplorer Ultimate ultrasound systems (V7.x to V12.x software versions)." Those are the product words and the software band. A scanner whose label uses different words, or whose displayed software is outside V7.x to V12.x, is not established as inside this letter by the SuperSonic name alone. 1

The public PDF address contains the filename "Aixplorer Gen II and Aixplorer Ultimate_End of Life Notice_May 10 2023.pdf." The letter text does not define Gen II, and it does not tell the reader to look for a Gen II mark on the chassis. Use the words that are printed on the system label and the software version the system displays. The letter does not give a menu path. Record the version string the console actually shows. 1

The same limit applies to connector counts. The letter says "4-connector." It does not describe connector shape, and it does not create a separate "2-connector Aixplorer" category. A catalog part whose name includes "2 interfaces" is a parts-list phrase, discussed later. It is not a second system family in this letter. 1

Words on the system labelSoftware the letter namesInside this letter?What is already known on 1 October 2026
Aixplorer 4-connectorV7.x to V12.xYesEnd of sale and the renewal cap are past. The seven-year sentence still needs the installation date.
Aixplorer UltimateV7.x to V12.xYesSame three clocks. The letter pairs Ultimate with the 4-connector scope sentence.
Aixplorer wording outside that sentence, or software outside V7.x to V12.xNot the named bandNot establishedDo not apply the letter from the brand name alone. Ask for the label and the version string.
MACH 10, MACH 20, MACH 30, or MACH 40Not namedNoThe letter only invites the reader to ask Hologic about SuperSonic MACH.
Who the 10 May 2023 letter names, checked against the letter text on 1 October 2026. FDA numbers in the next section identify trade names. They are not a software map.

Source: Hologic MISC-09014_Rev002.

How do the end-of-sale date, the 31 October 2023 contract cap, and the seven-year installation clock differ?

The letter does not set one shutdown day. It states three different clocks, and collapsing them is the usual reading error. 1

End of sale, 29 January 2021. The letter says: "Effective January 29, 2021, Aixplorer 4-connector and Aixplorer Ultimate ultrasound systems were declared End of Sale." That sentence declares end of sale. It does not state a manufacturing stop date, a warranty end date, or a parts-depletion date. Do not add those consequences from the words "end of sale" alone. 1

Contract renewals, capped at 31 October 2023. The next paragraph has three sentences, and they are not the same rule. "Ultrasound Solutions Corporation, a contracted service partner for Hologic, Inc., will continue to provide service for customers whose service contracts are currently in effect until their contract end date. Service contract renewals will be allowed through Ultrasound Solutions Corporation, and their end date will not exceed October 31, 2023. New contracts are not available." Existing contracts run to their own end dates. Renewals were still allowed, with an end date that will not exceed 31 October 2023. New contracts are not available. On 1 October 2026 that cap is about two years and eleven months in the past. The letter does not say that every SuperSonic system lost all OEM service on 31 October 2023, and it does not say the cap is a statute. 1

Best-effort corrective maintenance, seven years after installation. A separate sentence follows: "Best effort corrective maintenance will be provided for seven years post installation date." The letter does not define "best effort." It does not say which document proves installation, whether seven years is counted to the anniversary, or whether there is a grace period. It also does not say that the window is a post-warranty period or that it ends when a depot runs out of parts. Those are interpretations, not sentences in the letter. 1

Any seventh-anniversary date below is calendar arithmetic from the words "seven years post installation date." It is not a customer record and not a Hologic billing rule.

  • Seven calendar years after an illustrative installation on 1 June 2016 is 1 June 2023. That illustration is already past on 1 October 2026.
  • Seven calendar years after an illustrative installation on 15 September 2018 is 15 September 2025. That illustration is also already past.
  • Seven calendar years after an illustrative installation on 29 January 2021, the letter's end-of-sale date, is 29 January 2028. That illustration is still ahead on 1 October 2026.

The spread is the point. A 2019 installation is not automatically still inside the illustration: seven calendar years after 1 January 2019 is 1 January 2026, which is already past. A late installation near 29 January 2021 can still fall inside an anniversary illustration on 1 October 2026. The fleet is not uniformly open or uniformly closed. The multi-brand end-of-service playbook is the page for how to read an OEM letter across a mixed fleet. It does not parse this Hologic document. 1

No document checked for this page states whether Ultrasound Solutions Corporation still sells service in 2026. The letter remains the source for the renewal cap. It is not a current corporate-status report on that company.

ClockWhat the letter saysStatus on 1 October 2026What to verify before a service decision
End of saleAixplorer 4-connector and Aixplorer Ultimate systems were declared end of sale effective 29 January 2021.Past. The date is more than five years before the review date.Keep the sentence as an end-of-sale statement. Do not convert it into a warranty or parts end date the letter does not give.
Contract renewal capRenewals through Ultrasound Solutions Corporation may have an end date that will not exceed 31 October 2023. New contracts are not available. Contracts already in effect continue until their own end date.The cap date is past.Do not treat 31 October 2023 as the day every SuperSonic scanner lost corrective maintenance.
Best-effort corrective maintenanceBest effort corrective maintenance will be provided for seven years post installation date.Open or closed only after the installation date is known.Find the installation record. Label any anniversary math as an illustration. The letter does not define the counting rule.
The three clocks in MISC-09014_Rev002, read on 1 October 2026. Status describes the calendar, not a Hologic account lookup.

Source: Hologic letter dated 10 May 2023, MISC-09014_Rev002.

Does a MACH 10, 20, 30, or 40 system fall inside this letter?

No. The only MACH sentence in the letter is an invitation, not a coverage line: "If you are interested in learning more about our latest ultrasound product, SuperSonic MACH, please contact your local Hologic representative for more information." A summary that calls MACH the direct upgrade, or that drops the V7.x to V12.x band, is adding a recommendation and omitting a limit. The letter tells the reader to ask Hologic. It does not say MACH 10, 20, 30, or 40 is end of service, and it does not say MACH replaces every 4-connector system. 1

FDA 510(k) database pages separate the trade names. They do not supply the software band, and the letter does not cite them. Every record below lists applicant Supersonic Imagine, regulation 892.1550, classification product code IYN, subsequent product codes ITX and IYO, and a substantially equivalent decision. None of the pages states software V7.x to V12.x. Mapping K171105 or K173021 onto that band, or mapping K091970 or K132274 onto a V5 or V6 band, is not supported by these pages. 2 3 7 8

K180572, decided 29 May 2018, uses the device name AIXPLORER MACH Ultrasound Diagnostic Systems and the trade names Aixplorer Mach 30, Aixplorer Mach 20, and Aixplorer Mach 10. K202455, a Special 510(k) decided 29 December 2020, includes Aixplorer MACH20, Aixplorer MACH30, Supersonic MACH40, and related MACH20 and MACH30 names. That decision is before the letter's 29 January 2021 end-of-sale date, so MACH 40 is already on a clearance that predates the Aixplorer end-of-sale sentence. K203645, decided 29 June 2021, names Aixplorer MACH30/SUPERSONIC MACH30, Aixplorer MACH20/SUPERSONIC MACH20, and SUPERSONIC MACH40. Its decision date is after 29 January 2021. That sequence shows MACH clearances on both sides of the Aixplorer end-of-sale date. It is not a 2026 statement that OEM contracts for MACH remain available, and it is not a description of what the Special 510(k) changed. 4 5 6

The SUPERSONIC MACH 40 User's Guide, PM.LAB.126 Rev A, is a different document. It recommends annual maintenance by a Hologic authorized representative. It says all repairs must be conducted by a Hologic authorized representative. It also says the user can perform the maintenance operations described in its own Chapter 10. Those sentences belong to the MACH 40 guide. They do not amend MISC-09014, they do not make independent servicing unlawful, and this page does not copy Chapter 10. 12

510(k)Device name on the FDA pageDecision dateSummary typeSoftware on the pageCited by the 2023 letter?
K091970AIXPLORER ULTRASOUND SYSTEM12 August 2009TraditionalNot statedNo
K132274AIXPLORER24 September 2013SpecialNot statedNo
K171105AIXPLORER and AIXPLORER Ultimate Ultrasound Systems11 July 2017TraditionalNot statedNo
K173021Aixplorer and Aixplorer Ultimate Ultrasound Diagnostic Systems9 January 2018TraditionalNot statedNo
K180572AIXPLORER MACH Ultrasound Diagnostic Systems; Aixplorer Mach 30, 20, and 1029 May 2018TraditionalNot statedNo
K202455Aixplorer MACH20, Aixplorer MACH30, Supersonic MACH40, and related MACH20/30 names29 December 2020SpecialNot statedNo
K203645Aixplorer MACH30/SUPERSONIC MACH30, Aixplorer MACH20/SUPERSONIC MACH20, SUPERSONIC MACH4029 June 2021TraditionalNot statedNo
FDA 510(k) identity records checked on 1 October 2026. Decision dates are the database decision dates. Software version is blank on each of these pages, and MISC-09014 cites none of these submission numbers.

Source: FDA 510(k) database pages K091970, K132274, K171105, K173021, K180572, K202455, and K203645.

Why can a software version and installation date block a board quote?

The letter is a scope document. It becomes a parts order only after someone adds a part number the letter does not contain. Three missing facts are enough to stop that order. 1

The software string is the applicability test. V7.x to V12.x is the band the letter names. A quote that says only "Aixplorer" cannot show that the letter applies, and it cannot show that the letter does not apply. The 510(k) pages above do not fill that gap. They do not state a software version, so a clearance number is not a substitute for the version on the screen. 1 2

The installation date is the seven-year test. Without the date, and without the document that shows it, nobody can tell whether the best-effort sentence might still cover that serial. Buying a repair while that question is open can spend the budget before anyone has asked Hologic the question the letter itself points to breasthealth.support@hologic.com. The reverse is also true: an installation whose illustrative anniversary is already past is not a reason to invent a board. 1

The public catalog does not close the gap. It has one SuperSonic row. The part name is "PC(2 interfaces) SP00781." The model label is "SuperSonic." No manufacturer part number is listed. "2 interfaces" is the name of that row. It is not a 2-connector Aixplorer system, and it is not evidence that the part fits an Aixplorer 4-connector or Aixplorer Ultimate. Do not order it as a matched board. This page does not publish a symptom-to-board map, because that map is not in the letter and not in the catalog row.

Do not open an energized system, bypass an interlock, or defeat a protective earth to identify a board. Do not return a scanner to clinical use because an end-of-service letter has been read. Electrical-safety and performance checks belong to a qualified service provider and to the facility before clinical use. The boundary between servicing and remanufacturing is the subject of the FDA servicing and remanufacturing boundary, not a conclusion this Hologic letter can settle. 1

Which older Aixplorer notice is a disinfectant-list recall rather than this end-of-service letter?

Search results for Aixplorer service still surface Health Canada recall RA-71571. It is a different event. The starting date is 27 January 2012. The posting date is 2 April 2012. The hazard classification is Type II. The identification number on the page is RA-71571. The source-of-recall field says Health Canada. The reason says SuperSonic Imagine identified an error in the user's guide list of recommended cleaners and disinfectants. The disinfectants recommended for the SE12-3 are not all high-level disinfectants. The notice says the SE12-3 is used in a semi-critical application and should be cleaned and high-level disinfected after use. The affected-product heading calls it Probe SE12-3. The reason line on the archived page prints "SE12-3 Robe," which is the page's own wording next to that heading. 9

The catalog numbers on the notice are main unit SSIP90019, linear probe SSIP09002, curved array probe SSIP90030, and probe SE12-3 SSIP90068. The page does not describe a board failure, an end-of-sale date, or a service-contract cap. It also does not publish the corrective-action method, so this article does not invent a manual insert or a chemical list. Do not copy a disinfectant from a 2012 notice. Current probe reprocessing belongs to the current OEM instructions and to the probe high-level disinfection boundary. 9

A second false match is Hologic's public imaging obsolescence index. The HTML retrieved on 1 October 2026 has visible sections for screening and mammography, skeletal and bone-density systems, breast biopsy and surgery, workflow products, and Fluoroscan mini C-arm systems. That retrieved HTML contains no Aixplorer, SuperSonic, MACH, ultrasound, or MISC-09014 string. The direct PDF address for the 10 May 2023 letter still returned the letter. Absence from the index is not withdrawal of the PDF. The finding is limited to the HTML retrieved. It is not a claim about every Hologic template. 1 10

The same index links a newer letter that is easy to misread as an ultrasound update. Hologic's "US Product Components End of Support Notice," August 2026, REV 002 MISC-11752, is addressed to Breast and Skeletal Health Solutions customers. It discusses Microsoft Windows 10 IoT Enterprise 2016 LTSB and Windows Server Standard 2016 on named mammography, 3Dimensions, Trident HD, Fluoroscan InSight FD, Horizon DXA, SecurView, and Advanced Workflow Manager computers. Scheduled dates in that letter include 13 October 2026 and 12 January 2027. The letter does not name Aixplorer, SuperSonic, MACH, or ultrasound. It is not a revision of MISC-09014. 11

QuestionAixplorer letter MISC-09014_Rev002Health Canada RA-71571August 2026 notice MISC-11752
What kind of document is it?End-of-life and end-of-service customer letterType II medical device recall noticeOperating-system end-of-support letter
Date10 May 2023Starting 27 January 2012; posted 2 April 2012August 2026
Who it addressesHologic customers with the named Aixplorer systemsPublic recall notice. SuperSonic Imagine identified the user's-guide error.Breast and Skeletal Health Solutions customers
Products namedAixplorer 4-connector and Aixplorer Ultimate, software V7.x to V12.xMain unit SSIP90019, probes SSIP09002 and SSIP90030, probe SE12-3 SSIP90068Mammography, specimen radiography, mini C-arm, DXA, SecurView, and workflow computers
Decision it supportsApply the three clocks only after the label, software, and installation date matchDo not use it as an end-of-service letter or as a current disinfectant recipeDo not use it as an Aixplorer or MACH service letter
Three Hologic or regulator documents that can be confused with one another. Each row uses only the document named in that column.

Source: MISC-09014_Rev002, Health Canada RA-71571, the Hologic obsolescence index, and MISC-11752 Rev 002.

When does an Aixplorer service issue become a board or probe quote?

After the letter's scope is known, and not before. A symptom without a label is not yet a parts request. Use this order. 1

  1. Read the trade name on the rating plate. Record Aixplorer, Aixplorer Ultimate, or the MACH name that is actually printed. If the plate says MACH 10, 20, 30, or 40, stop using MISC-09014 as the service letter.
  2. Record the software version the system displays. If it is outside V7.x to V12.x, say so. Do not convert a 510(k) number into a software version.
  3. Find the installation date and the document that shows it. If the date is missing, the seven-year sentence cannot be applied. If the illustrative anniversary is still ahead, ask Hologic, at the address on the letter, whether best-effort corrective maintenance is still available for that serial before buying a private repair.
  4. Write the symptom in the operator's words. Include the error text on the screen. Do not relabel a dark image, a reboot, or a dead control panel as a named board.
  5. Separate an observation from a diagnosis. If a fault follows one probe across sockets, say that. If it stays with one socket across probes the site already trusts, say that. Those notes help a later review. They do not identify a channel board, a power supply, or a host computer.
  6. Photograph what is already visible. Photograph the system label. If a board is already out of the system, photograph both sides, including the etched part number and revision. Do not open an energized system to take the picture.

Where Rongtao fits, and where it does not

Rongtao Medical is not Hologic, not SuperSonic Imagine, and not Ultrasound Solutions Corporation. The 2023 letter names Ultrasound Solutions Corporation as a contracted service partner for the contracts it describes. It does not appoint an independent service company, and it does not authorize Rongtao to act for Hologic. 1

On this site, SuperSonic is an on-request brand. The published model line is Aixplorer and Mach, on request. Coverage is limited and is scoped case by case. SuperSonic is outside the core brand list. The core list includes GE Healthcare, Philips, Siemens / Acuson, Hitachi, Mindray, Samsung Medison, Toshiba (Canon), Aloka, and Biosound Esaote. OEM names on that list identify equipment Rongtao services. They are not an authorization or an endorsement by those manufacturers. The brand route is SuperSonic on-request coverage.

Where a scoped repair is accepted, the published service facts are general, not Aixplorer-specific. The repair center is a 3,000 m² technical and warehousing center in Guangzhou. The engineering figure is 35+ senior engineers. Service spans 140+ countries. Every repaired board runs for 48 hours inside an actual ultrasound system before release. Typical board-repair turnaround is 5 to 8 business days. The typical warranty is 90 days, with the final term confirmed by the item and the service. Those sentences are not a stock promise, a price, a repairability rate, or a success rate for Aixplorer. The service overview is ultrasound repair services.

Quote-ready technical handoff checklist

Send the case through contact with the items below. "Aixplorer board needed" is not a quotable request.

  1. Trade name printed on the system label, and the serial number.
  2. Software version string copied from the system, not from a 510(k) number.
  3. Installation date, and the acceptance sheet or other record that shows it.
  4. Symptom and any error text, in the operator's words.
  5. Photos of the system label. If a board is already removed, photos of both sides and the etched part number.
  6. Whether the fault followed one probe or stayed with one socket.
  7. Quantity and destination country.

Frequently asked questions

Did every SuperSonic ultrasound lose OEM service on 31 October 2023?
No. In MISC-09014_Rev002, 31 October 2023 is the date a renewal end date will not exceed. Contracts already in effect continue until their own end date. New contracts are not available. Best-effort corrective maintenance is a separate sentence: seven years post installation date. The letter does not put MACH 10, 20, 30, or 40 under either clock. 1

Does the 2023 letter declare SuperSonic MACH systems end of service?
No. MACH appears in one invitation to contact a local Hologic representative. K180572, K202455, and K203645 are separate FDA trade-name records. K202455 already includes a MACH 40 name on 29 December 2020, before the Aixplorer end-of-sale date. None of those records is a 2026 contract promise. 1 4 6

Is the 2012 Health Canada Aixplorer notice the same event as the 2023 letter?
No. RA-71571 is a Type II recall starting 27 January 2012. The stated reason is an error in the user's guide list of recommended cleaners and disinfectants for the SE12-3, which the notice says is used in a semi-critical application. It is not an end-of-service letter and not a current disinfection procedure. 9

Can catalog row SP00781 be ordered as an Aixplorer board?
No. The only public SuperSonic catalog row is named PC(2 interfaces) SP00781. The model label is SuperSonic, and no manufacturer part number is listed. That row is not a verified Aixplorer 4-connector or Ultimate part.

Does the letter authorize an independent service company to act for Hologic?
No. It names Ultrasound Solutions Corporation as a contracted service partner for the contracts the letter describes. It does not appoint or endorse another service company. Rongtao Medical does not claim that role. 1

How should an HTM team test the seven-year sentence?
Find the installation record and add seven calendar years as an illustration only. If that illustration is still ahead on the day of the decision, ask Hologic whether best-effort corrective maintenance is available for that serial. If the illustration is already past, the letter's renewal cap is also past, and a private repair still needs the label, software, symptom, and part photos. The letter does not define the anniversary convention. 1

Sources

  1. Hologic: Product End of Life Notice and End of Service for Aixplorer 4-connector systems (Aixplorer and Aixplorer Ultimate), 10 May 2023, footer reference MISC-09014_Rev002. Read 1 October 2026.
  2. U.S. FDA 510(k) K173021, device name Aixplorer and Aixplorer Ultimate Ultrasound Diagnostic Systems, applicant Supersonic Imagine, decision date 9 January 2018, substantially equivalent, product code IYN with subsequent codes ITX and IYO, regulation 892.1550. The database page does not state a software version.
  3. U.S. FDA 510(k) K171105, device name AIXPLORER and AIXPLORER Ultimate Ultrasound Systems, applicant Supersonic Imagine, traditional 510(k), decision date 11 July 2017, substantially equivalent. The database page does not state a software version.
  4. U.S. FDA 510(k) K180572, device name AIXPLORER MACH Ultrasound Diagnostic Systems, with Aixplorer Mach 30, Aixplorer Mach 20, and Aixplorer Mach 10, applicant Supersonic Imagine, decision date 29 May 2018, substantially equivalent.
  5. U.S. FDA 510(k) K203645, device name Aixplorer MACH30/SUPERSONIC MACH30, Aixplorer MACH20/SUPERSONIC MACH20, and SUPERSONIC MACH40, applicant Supersonic Imagine, decision date 29 June 2021, substantially equivalent.
  6. U.S. FDA 510(k) K202455, Special 510(k), device name includes Aixplorer MACH20, Aixplorer MACH30, Supersonic MACH40, Supersonic MACH30, and a MACH20 name, applicant Supersonic Imagine, decision date 29 December 2020, substantially equivalent. This page is used for trade-name identity only.
  7. U.S. FDA 510(k) K091970, device name AIXPLORER ULTRASOUND SYSTEM, applicant Supersonic Imagine, decision date 12 August 2009, substantially equivalent. The database page does not state a software version.
  8. U.S. FDA 510(k) K132274, Special 510(k), device name AIXPLORER, applicant Supersonic Imagine, decision date 24 September 2013, substantially equivalent. The database page does not state a software version or describe the change cleared.
  9. Health Canada medical device recall RA-71571, starting date 27 January 2012, posting date 2 April 2012, hazard classification Type II. The stated reason is an error in the user's guide list of recommended cleaners and disinfectants for the SE12-3, which the notice says is used in a semi-critical application. Catalog numbers on the notice: main unit SSIP90019, linear probe SSIP09002, curved array probe SSIP90030, and probe SE12-3 SSIP90068.
  10. Hologic Imaging Product Obsolescence and End-of-Life Guide, public index retrieved 1 October 2026. Visible headings include Screening, Skeletal, Breast Biopsy / Surgery, and workflow documents. The retrieved HTML contained no Aixplorer, SuperSonic, MACH, ultrasound, or MISC-09014 string.
  11. Hologic: US Product Components End of Support Notice, August 2026, REV 002 MISC-11752, addressed to Breast and Skeletal Health Solutions customers. It covers named mammography, specimen-radiography, mini C-arm, DXA, SecurView, and workflow computers on Windows 10 IoT Enterprise 2016 LTSB or Windows Server Standard 2016. It does not name Aixplorer, SuperSonic, MACH, or ultrasound.
  12. Hologic: SUPERSONIC MACH 40 User's Guide, PM.LAB.126 Rev A. The guide recommends annual maintenance by a Hologic authorized representative, states that all repairs must be conducted by a Hologic authorized representative, and says the user can perform the maintenance operations described in its Chapter 10. Those sentences are not the 2023 Aixplorer letter.

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