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Tekdyne

Country not established

Devices
1

What Tekdyne makes

Tekdyne makes medical devices such as the TEKDYNE MICRO RETRACTOR, which is a type of surgical instrument.

The company's portfolio is regulated as Class I devices and is listed in the FDA 510(k) registry, with the company based in the US.

AI-generated from registry data, 21 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Tekdyne Micro Retractor Ref K910975

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

Frequently asked questions

How many devices does Tekdyne have in the registry?

The registry currently lists 1 device for Tekdyne. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tekdyne's devices?

Among its 1 most recently registered device, Tekdyne has devices listed in FDA 510(k) (1 device).

What risk classes do Tekdyne's devices fall under?

Among its 1 most recently registered device, the classes recorded for Tekdyne's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Tekdyne in the registry?

The most recently registered devices listed for Tekdyne include TEKDYNE MICRO RETRACTOR.

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