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Wright Medical Technology, Inc.

Active in EUDAMED
Also registered as Wright Medical Technology

United Statesfrom SRN EUDAMED FDA SRN US-MF-000025260 FEI 1043534

Wright Medical Technology, Inc. is a medical device manufacturer based in the United States, with 9,097 devices listed and 141 FDA recalls as of 12 Nov 2026.

Devices
9,097
Registrations
EUDAMEDFDA
FDA recalls
14115 ongoing

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 2,846
  • EUDAMED 1,571

Among the 3,000 best-ranked of 9,097 devices.

Device classes
  • FDA Class II 2,186
  • FDA Class I 658
  • EU Class IIb 134
  • EU Class IIa 18
  • EU Class I 3

Among the 3,000 best-ranked of 9,097 devices.

Top EMDN categories

Among the 3,000 best-ranked of 9,097 devices.

FDA recalls
Sites and related companies
Identifiers
  • EUDAMED SRN US-MF-000025260
  • FDA FEI 1043534
  • DUNS 807201207

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI, FDA recalls
Authorised rep.
Stryker European Operations LimitedIE

What Wright Medical Technology, Inc. makes

The company manufactures orthopaedic bone screws, including non-bioabsorbable and non-sterile variants, as well as non-sliding types for surgical fixation. It also produces fixed-bearing total ankle prostheses, reusable surgical implant templates, and ankle prosthesis trials. Orthopaedic fixation plates, both non-bioabsorbable and non-sterile, are part of its portfolio, alongside specific device examples like the Incompass Total Ankle System and TCP.

These devices are regulated under FDA Class I and Class II classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9,097

Newest first, rows 1-50 of 9,097

Search and filter all 9,097 devices
Skip device list

  • Invision Ref 60002030

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Ortholoc® 3Di Ref 58880060

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc 3Di Ref 58T7001L

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Inbone® Ref 22037002

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Invision Ref 60001510

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb

  • Invision® Ref 60016627

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc® 3Di Crosscheck® Ref 5820003

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc® 3Di Ref 59250078

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc 3Di Ref 58T30008

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Ortholoc 3Di Ref 58T40065

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Swanson™ Ref 24240000

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Charlotte® Ref 43511035

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Invision Ref 61002010

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb

  • CLAW ll Ref 402T1320

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • CLAW ll Ref 402T1425

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision Ref 60610000S

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb

  • Dart-Fire® Ref DSDS1050S

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Ortholoc 3Di Ref 58T30010

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Ortholoc 3Di Ref 58T50001

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Infinity® Ref SMS00426

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Invision® Ref 60016611

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc 3Di Ref 58T338LT

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision Ref 60002031

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Ortholoc® 3Di Ref 58885100

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Invision Ref 60002040

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • PROstep® Solo Guide Ref 57790CAD

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Invision® Ref 60016614

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Charlotte® Ref 43110011

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc® 3Di Ref 59250075

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Invision Ref 60002050

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Evolve® Ref 49510128

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Charlotte® Ref 45112002

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc 3Di Ref 58T7003R

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision Ref 60002051

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Pro-Toe® Ref 45719000

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc 3Di Ref 58T7002L

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision™ Ref 60611000

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Charlotte® Ref 44122006

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • CLAW ll Ref 402T1420

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision Ref 6000214L

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb

  • Invision® Ref 60016615

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc® 3Di Ref 58880100

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc 3Di Ref 58T50002

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision Ref 60002041

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision® Ref 60016625

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc® 3Di Ref 59250076

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Ortholoc 3Di Ref 58T80000

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Invision Ref 6000213R

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb

  • Invision Ref 60002020

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Ortholoc 3Di Ref 58T60003

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

Rows 1-50 of 9,097

Showing 1-50 of 9,097

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000025260
FDA FEI number
1043534
DUNS number
807201207
EUDAMED status
Active
EUDAMED registered name
Wright Medical Technology, Inc.
Registered address
11500, Memphis-Arlington Road, 38002, Tennessee, United States
Phone
+41 (0)32 641 6666
PRRC contact
Jeanine Redden(public in EUDAMED)

FDA recalls141

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 141 recalls initiated by WRIGHT MEDICAL TECHNOLOGY, INC., the earliest on 2003-08-18 and the most recent on 2026-08-18. By recorded status: 15 ongoing and 126 terminated. The reasons filed fall into these groups: labeling or instructions for use, sterility or contamination, packaging, mechanical integrity and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

  • 2017 0
  • 2018 2
  • 2019 2
  • 2020 4
  • 2021 5
  • 2022 10
  • 2023 5
  • 2024 1
  • 2025 0
  • 2026 1

111 initiated before 2017

Showing the 10 most recent of 141 recalls.

  • 2026

    • 18 Aug 2026 Z-3334-2026 Class II Ongoing Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used would prevent a secure rigid engagement with the plate's internal threads, which may lead to surgery prolongation to retrieve another device, or alternative surgery method if no replacement device is readily available. Distribution: US Nationwide distribution in the states of FL, TX, PA, CA, ID, MI, OK, TN, NJ, WI, CO. Submission number: K133715

  • 2024

    • 6 Mar 2024 Z-1477-2024 Class II Ongoing Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide. Distribution: US: TX, NE, and AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHINA, COLOMBIA, FRANCE, GERMANY, ITALY, SPAIN, SWEDEN, SWITZERLAND,…
      Full distribution text US: TX, NE, and AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHINA, COLOMBIA, FRANCE, GERMANY, ITALY, SPAIN, SWEDEN, SWITZERLAND, UK
      Submission number: K123954

  • 2023

    • 13 Jun 2023 Z-2105-2023 Class II Ongoing The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes. Distribution: There was no U.S. distribution, including government and military. Foreign distribution was made to Australia, Belgium,…
      Full distribution text There was no U.S. distribution, including government and military. Foreign distribution was made to Australia, Belgium, Canada, Chile, China, Colombia, France, Germany, Italy, Mexico, Netherlands, Spain, Sweden, Switzerland, Taiwan, and the United Kingdom.
      Submission number: K123954
    • 10 Apr 2023 Z-1466-2023 Class II Ongoing Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts. Distribution: US Nationwide distribution. Submission number: K120359
    • 10 Apr 2023 Z-1467-2023 Class II Ongoing Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts. Distribution: US Nationwide distribution. Submission number: K120359
    • 2 Feb 2023 Z-1169-2023 Class II Ongoing Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa. Distribution: US Nationwide distribution in the state of NY. Submission number: K113014
    • 2 Feb 2023 Z-1170-2023 Class II Ongoing Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa. Distribution: US Nationwide distribution in the state of NY. Submission number: K113014

  • 2022

    • 30 Sep 2022 Z-0139-2023 Class II Terminated The tibial tray lock detail is oversized (larger than specification). Distribution: US Nationwide distribution in the state of New York. Submission number: K051023
    • 30 Sep 2022 Z-0140-2023 Class II Terminated The tibial tray lock detail is oversized (larger than specification). Distribution: US Nationwide distribution in the state of New York. Submission number: K051023
    • 3 Aug 2022 Z-0005-2023 Class II Ongoing The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem 9.5mm +4 contains a size 7.5mm +2 stem. Distribution: US Nationwide distribution. Submission numbers: K060731, K991915
Show the 25 most recent of 141 recalls

  • 2022

    • 3 Aug 2022 Z-0006-2023 Class II Ongoing The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem 9.5mm +4 contains a size 7.5mm +2 stem. Distribution: US Nationwide distribution. Submission numbers: K060731, K991915
    • 27 Jul 2022 Z-1567-2022 Class II Ongoing An incorrect sizing label was applied to the carton packaging. Distribution: Worldwide distribution - US Nationwide distribution in the states of AZ, CA, FL, GA, NY, PA, and TN. The countries of…
      Full distribution text Worldwide distribution - US Nationwide distribution in the states of AZ, CA, FL, GA, NY, PA, and TN. The countries of the Australia, France, the Netherlands, Sweden, and the United Kingdom.
    • 14 Jun 2022 Z-1366-2022 Class II Ongoing The plate cutter is unable to meet sterilization requirements when it is sterilized in a double-wrapped configuration according to the Option 1 Steam Sterilization parameters detailed in instructions for use Distribution: Nationwide and PR, and Australia, Canada, Chile, Colombia, Hong Kong, Puerto Rico
    • 2 Jun 2022 Z-1291-2022 Class II Ongoing The instrument is incorrectly color coded. Distribution: Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IA, IL, MA, MI, MN, MO, NC,…
      Full distribution text Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IA, IL, MA, MI, MN, MO, NC, NY, OH, PA, TX, and WA. The countries of Australia, Belgium, Canada, France, Germany, Hong Kong, Israel, Sweden, Switzerland, and United Kingdom.
      Submission number: K140749
    • 10 Mar 2022 Z-0853-2022 Class II Terminated The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking. Distribution: US distribution to Florida, North Carolina, Ohio, and Texas Submission number: K203832
    • 15 Feb 2022 Z-0786-2022 Class II Terminated An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw. Distribution: International distribution to the country of France. Submission number: K090692
    • 9 Feb 2022 Z-0679-2022 Class II Terminated Product was labelled with the incorrect manufacturing and distribution dates. Distribution: International distribution in the countries of Japan and the United Kingdom. Submission number: K061808

  • 2021

    • 3 Dec 2021 Z-0392-2022 Class II Ongoing The incorrect product is contained in the packaging. Distribution: Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany,…
      Full distribution text Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.
      Submission number: K113014
    • 3 Dec 2021 Z-0393-2022 Class II Ongoing The incorrect product is contained in the packaging. Distribution: Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany,…
      Full distribution text Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.
      Submission number: K061808
    • 3 Dec 2021 Z-0401-2022 Class II Ongoing Incorrect product is contained in the packaging. Distribution: Worldwide distribution - US Nationwide distribution in the states of AZ, IA, and SC. The countries of Australia, Canada,…
      Full distribution text Worldwide distribution - US Nationwide distribution in the states of AZ, IA, and SC. The countries of Australia, Canada, Chile, Spain, and United Kingdom.
      Submission number: K141417
    • 4 Nov 2021 Z-0315-2022 Class II Terminated The package contents and package labeling do not match. Distribution: US Nationwide distribution in the states of MI and PA. Submission number: K100886
    • 4 Nov 2021 Z-0316-2022 Class II Terminated The package contents and package labeling do not match. Distribution: US Nationwide distribution in the states of MI and PA. Submission number: K100886

  • 2020

    • 26 Aug 2020 Z-2989-2020 Class II Terminated Lack of sterility assurance Distribution: USA states: CA, CO, FL, GA, MA, MO, OH, PA, TX OUS: Australia, Canada, Chile, Israel, Spain Submission numbers: K060731, K991915
    • 28 Jul 2020 Z-2796-2020 Class II Terminated Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws. Distribution: US Nationwide distribution including in the states of CO, TX, OR, KX, SC, CA, AR, NJ, UT, VA, MO, NC, FL, IL.
    • 28 Jul 2020 Z-2797-2020 Class II Terminated Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws. Distribution: US Nationwide distribution including in the states of CO, TX, OR, KX, SC, CA, AR, NJ, UT, VA, MO, NC, FL, IL.

Frequently asked questions

How many devices does WRIGHT MEDICAL TECHNOLOGY, INC. have in the registry?

The registry currently lists 9097 devices for WRIGHT MEDICAL TECHNOLOGY, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list WRIGHT MEDICAL TECHNOLOGY, INC.'s devices?

Among its 50 most recently registered devices, WRIGHT MEDICAL TECHNOLOGY, INC. has devices listed in EUDAMED (50 devices).

What risk classes do WRIGHT MEDICAL TECHNOLOGY, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for WRIGHT MEDICAL TECHNOLOGY, INC.'s devices are Class I, Class IIa and Class IIb. Each device page shows its own class and authorisation.

Are there FDA recall records for WRIGHT MEDICAL TECHNOLOGY, INC.?

FDA recall records list 141 recalls initiated by WRIGHT MEDICAL TECHNOLOGY, INC., the most recent initiated on 18 Aug 2026. 15 of them are recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from WRIGHT MEDICAL TECHNOLOGY, INC. in the registry?

The most recently registered devices listed for WRIGHT MEDICAL TECHNOLOGY, INC. include INVISION, Ortholoc® 3Di, Ortholoc 3Di and Inbone®.

Generated automatically from registry data and not verified by a human reviewer.