Medical Device Manufacturer · US , Pawtucket , RI

Medworks Corp.

3 submissions · 3 cleared · Since 1998
3
Total
3
Cleared
0
Denied

Medworks Corp. — FDA 510(k) Submissions

Medworks Corp. has submitted 3 FDA 510(k) premarket notifications since 1998, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cannula, Intrauterine Insemination, Catheter, Retention Type, Balloon . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 Obstetrics & Gynecology 2 Gastroenterology & Urology 1