Medical Device Manufacturer · US , Washington, Dc , DC

Glasspan, Inc.

1 submissions · 1 cleared · Since 1994
1
Total
1
Cleared
0
Denied

Glasspan, Inc. — FDA 510(k) Submissions

Glasspan, Inc. has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Splint, Endodontic Stabilizing . Use the specialty filter in the sidebar to narrow results.

1 devices
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