Medical Device Manufacturer · US , Minneapolis , MN

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

6 submissions · 5 cleared · Since 1985

Total

Cleared

Denied

Surgidyne, Inc. has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 5 cleared submissions from 1985 to 1989. Primary specialty: General & Plastic Surgery.

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

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

6 devices

1-6 of 6