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Numedtec, Inc.

United StatesFDA applicant, unverified

Devices
2

What Numedtec, Inc. makes

Numedtec, Inc. manufactures a support pump designed for medical applications, as well as a support ring intended for orthopedic or spinal stabilization procedures.

The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The products are based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Support Pump Ref K904486

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Support Ring Ref K904485

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

Frequently asked questions

How many devices does Numedtec, Inc. have in the registry?

The registry currently lists 2 devices for Numedtec, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Numedtec, Inc.'s devices?

Among its 2 most recently registered devices, Numedtec, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Numedtec, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Numedtec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Numedtec, Inc. in the registry?

The most recently registered devices listed for Numedtec, Inc. include SUPPORT PUMP and SUPPORT RING.

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