Medical Device Manufacturer · US , Canton , MA

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

12 submissions · 12 cleared · Since 1997
12
Total
12
Cleared
0
Denied

Organogenesis, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Canton, US.

Last cleared in 2023. Active since 1997.

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) cleared devices by Organogenesis, Inc.

12 devices
1-12 of 12
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