Medical Device Manufacturer · US , Stratford , CT

Surgicon, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Surgicon, Inc. has 2 FDA 510(k) cleared medical devices. Based in Stratford, US.

Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Surgicon, Inc. Filter by specialty or product code using the sidebar.

Surgicon, Inc. is one of 25763 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Surgicon, Inc.

2 devices

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