Medical Device Manufacturer · US , Minneapolis , MN

Gyrus Medical, Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 2002
15
Total
15
Cleared
0
Denied

Gyrus Medical, Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Minneapolis, US.

Historical record: 15 cleared submissions from 2002 to 2005.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Gyrus Medical, Inc.

15 devices
1-12 of 15
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