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Transcoject GmbH & Co. KG

GermanyFDA applicant, unverified

Devices
1

What Transcoject GmbH & Co. KG makes

Transcoject GmbH & Co. KG manufactures disposable plastic syringes, designed for single-use medical injections and fluid administration in clinical and homecare settings.

Their product portfolio is regulated under FDA 510(k) clearance as Class II devices. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Disposable Plastic Syringes Ref K851523

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

Frequently asked questions

How many devices does Transcoject GmbH & Co. KG have in the registry?

The registry currently lists 1 device for Transcoject GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Transcoject GmbH & Co. KG's devices?

Among its 1 most recently registered device, Transcoject GmbH & Co. KG has devices listed in FDA 510(k) (1 device).

What risk classes do Transcoject GmbH & Co. KG's devices fall under?

Among its 1 most recently registered device, the classes recorded for Transcoject GmbH & Co. KG's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Transcoject GmbH & Co. KG in the registry?

The most recently registered devices listed for Transcoject GmbH & Co. KG include DISPOSABLE PLASTIC SYRINGES.

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