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Ni-Med, Inc.

United StatesFDA applicant, unverified

Devices
3

What Ni-Med, Inc. makes

Ni-Med, Inc. makes I.V. start kits, suction catheters, and P. urine meters with a 250cc capacity.

These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • I.V. Start Kits Ref K875315

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Suction Catheter Ref K981910

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • P. Urine Meter, 250cc Ref K872824

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

Frequently asked questions

How many devices does Ni-Med, Inc. have in the registry?

The registry currently lists 3 devices for Ni-Med, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ni-Med, Inc.'s devices?

Among its 3 most recently registered devices, Ni-Med, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Ni-Med, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Ni-Med, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ni-Med, Inc. in the registry?

The most recently registered devices listed for Ni-Med, Inc. include I.V. START KITS, SUCTION CATHETER and P. URINE METER, 250CC.

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