Medical Device Manufacturer · US , Paterson , NJ

Glederer & Co., Inc.

2 submissions · 2 cleared · Since 1996
2
Total
2
Cleared
0
Denied

Glederer & Co., Inc. — FDA 510(k) Submissions

Glederer & Co., Inc. has submitted 2 FDA 510(k) premarket notifications since 1996, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include LDQ . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 General & Plastic Surgery 2