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Berkeley Bio-Medical, Inc.

United StatesFDA applicant, unverified

Devices
2

What Berkeley Bio-Medical, Inc. makes

Berkeley Bio-Medical, Inc. manufactures IDENTI-CLAMPS and IDENTI-LOOPS, which are medical devices used for securing or identifying medical tubing or catheters in clinical settings.

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

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Identi-Clamps Ref K780721

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Identi-Loops Ref K780720

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

Frequently asked questions

How many devices does Berkeley Bio-Medical, Inc. have in the registry?

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

Which registries list Berkeley Bio-Medical, Inc.'s devices?

Among its 2 most recently registered devices, Berkeley Bio-Medical, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Berkeley Bio-Medical, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Berkeley Bio-Medical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Berkeley Bio-Medical, Inc. in the registry?

The most recently registered devices listed for Berkeley Bio-Medical, Inc. include IDENTI-CLAMPS and IDENTI-LOOPS.

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