Vitromed GmbH

Vitromed GmbH — FDA 510(k) Submissions

Vitromed GmbH has submitted 7 FDA 510(k) premarket notifications since 2020, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media, Reproductive, Microtools, Assisted Reproduction (pipettes) . Use the specialty filter in the sidebar to narrow results.