Skip to content

Zeppelin Medizinlechnik GmbH

Country not established

Devices
1

What Zeppelin Medizinlechnik GmbH makes

Zeppelin Medizinlechnik GmbH manufactures non-compressive obstetric forceps, designed for assisted vaginal deliveries to aid in the safe delivery of babies.

The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer 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

  • Forceps, Ob, Non-Compressive Ref K771106

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

Frequently asked questions

How many devices does Zeppelin Medizinlechnik GmbH have in the registry?

The registry currently lists 1 device for Zeppelin Medizinlechnik GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Zeppelin Medizinlechnik GmbH's devices?

Among its 1 most recently registered device, Zeppelin Medizinlechnik GmbH has devices listed in FDA 510(k) (1 device).

What risk classes do Zeppelin Medizinlechnik GmbH's devices fall under?

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

What are the newest devices from Zeppelin Medizinlechnik GmbH in the registry?

The most recently registered devices listed for Zeppelin Medizinlechnik GmbH include FORCEPS, OB, NON-COMPRESSIVE.

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