Medical Device Manufacturer · US , Cambridge , MA

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

18 submissions · 17 cleared · Since 2007
18
Total
17
Cleared
1
Denied

Tepha, Inc. has 17 FDA 510(k) cleared general & plastic surgery devices. Based in Cambridge, US.

Latest FDA clearance: Apr 2024. Active since 2007.

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 - Tepha, Inc.
18 devices
1-12 of 18
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