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Dt Medtech, LLC

Country not established

Devices
402
FDA recalls
31 ongoing

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Dt Medtech, LLC makes

Dt Medtech, LLC manufactures prosthetic components for ankle replacements, including ankle prosthesis bearings, coated tibia and talus prostheses, and reusable trial components for fitting. Their portfolio also includes reusable surgical instruments such as drill guides, orthopaedic alignment tools, screwdrivers, and implant impactors, designed for orthopaedic procedures.

The company’s devices are classified under FDA’s Class I, Class II, and Class III categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

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

Catalogue402

Newest first, rows 1-50 of 402

Search and filter all 402 devices
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  • Hintermann Series 319692

    Listed Registry: GUDID Class:I

  • Hintermann Series 319865

    Listed Registry: GUDID Class:I

  • Hintermann Series 319866

    Listed Registry: GUDID Class:I

  • Hintermann Series 319867

    Listed Registry: GUDID Class:I

  • Hintermann Series 329646

    Listed Registry: GUDID Class:I

  • Hintermann Series 399900

    Listed Registry: GUDID Class:I

  • Hintermann Series H2 321806

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 422836

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 322107

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series 319693

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series 309637

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series H2 421825

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H3 300509 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series H2 322507

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 321316

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 401125

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 322227

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 322116

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 421803

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series 319798

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series H3 300306 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series 319005

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series H2 322206

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 321605

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series 309655

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series H2 321836

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series 309635

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series H2 322505

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 321917

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H3 300605 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series H2 321415

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 322225

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H3 300407 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series H2 401113

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 322306

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series 319765

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series H2 321327

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H3 302123 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series 309302

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Hintermann Series H2 322506

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H3 302206 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series H2 322519

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H3 300409 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series H2 322219

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H3 302124 Open recall

    Active Regimes: PMA Registry: GUDID Class:III

  • Hintermann Series H2 322616

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 321107

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 322105

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 321125

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Hintermann Series H2 322806

    Active Regimes: 510(k) Registry: GUDID Class:II

Rows 1-50 of 402

Showing 1-50 of 402

Company details

DUNS number
080101891
Phone
800-521-5002

FDA recalls3

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

FDA recall records list 3 recalls initiated by Dt Medtech, LLC, the earliest on 2018-09-25 and the most recent on 2026-03-24. By recorded status: 1 ongoing and 2 terminated. The reasons filed fall into these groups: labeling or instructions for use and packaging. 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 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 1

  • 2026

    • 24 Mar 2026 Z-2399-2026 Class II Ongoing Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device. Distribution: Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR. Submission number: P160036

  • 2018

    • 25 Sep 2018 Z-0402-2019 Class II Terminated Incorrect package labeling identifying the device Distribution: Australia, Ireland, Korea, Germany
    • 25 Sep 2018 Z-0403-2019 Class II Terminated Incorrect package labeling identifying the device Distribution: Australia, Ireland, Korea, Germany

Frequently asked questions

How many devices does Dt Medtech, LLC have in the registry?

The registry currently lists 402 devices for Dt Medtech, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dt Medtech, LLC's devices?

Among its 50 most recently registered devices, Dt Medtech, LLC has devices listed in FDA GUDID (50 devices).

What risk classes do Dt Medtech, LLC's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Dt Medtech, LLC's devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

Are there FDA recall records for Dt Medtech, LLC?

FDA recall records list 3 recalls initiated by Dt Medtech, LLC, the most recent initiated on 24 Mar 2026. 1 of them is 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 Dt Medtech, LLC in the registry?

The most recently registered devices listed for Dt Medtech, LLC include Hintermann Series 319692, Hintermann Series 319865, Hintermann Series 319866 and Hintermann Series 319867.

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