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Innomed Healthscience, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3014941496

Devices
1
Registrations
FDA
FDA recalls
0

What Innomed Healthscience, Inc. makes

INNOMED HEALTHSCIENCE, INC. manufactures the Bongo device, which is classified as a Class II medical device.

The company is based in the US and the Bongo device is listed in the FDA 510(k) registry.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Bongo Ref K180619

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

Company details

FDA FEI number
3014941496
Address
1701 W. Hillsboro Blvd, Deerfield Bch, FL, 33442

Frequently asked questions

How many devices does INNOMED HEALTHSCIENCE, INC. have in the registry?

The registry currently lists 1 device for INNOMED HEALTHSCIENCE, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list INNOMED HEALTHSCIENCE, INC.'s devices?

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

What risk classes do INNOMED HEALTHSCIENCE, INC.'s devices fall under?

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

What are the newest devices from INNOMED HEALTHSCIENCE, INC. in the registry?

The most recently registered devices listed for INNOMED HEALTHSCIENCE, INC. include Bongo.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.