Medical Device Manufacturer · US , New Britain , CT

Kelyniam Global, Inc.

4 submissions · 4 cleared · Since 2011
4
Total
4
Cleared
0
Denied

Kelyniam Global, Inc. — FDA 510(k) Submissions

Kelyniam Global, Inc. has submitted 4 FDA 510(k) premarket notifications since 2011, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Cranioplasty, Preformed, Non-alterable, Plate, Cranioplasty, Preformed, Alterable . Use the specialty filter in the sidebar to narrow results.

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All4 Neurology 4