Medical Device Manufacturer · US , New Port Richey , FL

Bergen Mfg.

4 submissions · 4 cleared · Since 1986
4
Total
4
Cleared
0
Denied

Bergen Mfg. — FDA 510(k) Submissions

Bergen Mfg. has submitted 4 FDA 510(k) premarket notifications since 1986, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Apparatus, Electrosurgical . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 General & Plastic Surgery 4