Medical Device Manufacturer · US , Durham , NC

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

15 submissions · 15 cleared · Since 2009
15
Total
15
Cleared
0
Denied

Transenterix, Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Durham, US.

Last cleared in 2021. Active since 2009.

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 Transenterix, Inc.

15 devices
1-12 of 15
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