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Venture Management Corp.

United StatesFDA applicant, unverified

Devices
3

What Venture Management Corp. makes

Venture Management Corp. manufactures the DELTA, a Class I/II medical device, the GELFLEX, a flexible gel-based product for medical applications, and the LYELL SOUND, an auditory or acoustic device.

The company’s portfolio includes devices regulated under the FDA’s 510(k) pathway, with products classified as Class I and Class II. These devices are listed in the FDA’s 510(k) registry, and the company is based in the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Delta Ref K943178

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Gelflex Ref K940848

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Lyell Sound Ref K954972

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

Frequently asked questions

How many devices does Venture Management Corp. have in the registry?

The registry currently lists 3 devices for Venture Management Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Venture Management Corp.'s devices?

Among its 3 most recently registered devices, Venture Management Corp. has devices listed in FDA 510(k) (3 devices).

What risk classes do Venture Management Corp.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Venture Management Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Venture Management Corp. in the registry?

The most recently registered devices listed for Venture Management Corp. include DELTA, GELFLEX and LYELL SOUND.

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