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Kershenstine Diamond, Inc.

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Devices
1

What Kershenstine Diamond, Inc. makes

Kershenstine Diamond, Inc. makes medical devices such as the TS1 TURTLE(TM) SYRINGE, which is a type of syringe.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • TS1 Turtle(Tm) Syringe Ref K936225

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

Frequently asked questions

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

The registry currently lists 1 device for Kershenstine Diamond, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kershenstine Diamond, Inc.'s devices?

Among its 1 most recently registered device, Kershenstine Diamond, Inc. has devices listed in FDA 510(k) (1 device).

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

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

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

The most recently registered devices listed for Kershenstine Diamond, Inc. include TS1 TURTLE(TM) SYRINGE.

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