Transenterix, Inc. - FDA 510(k) Cleared Devices
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
Cleared
Mar 02, 2021
Senhance Surgical System
General & Plastic Surgery
211d
Cleared
Mar 09, 2020
Senhance Surgical System
General & Plastic Surgery
60d
Cleared
Nov 22, 2019
Senhance Surgical System
General & Plastic Surgery
45d
Cleared
Jul 11, 2019
Senhance Surgical System
General & Plastic Surgery
37d
Cleared
Jan 11, 2019
Senhance Ultrasonic System
General & Plastic Surgery
128d
Cleared
Dec 06, 2018
Senhance Surgical System
General & Plastic Surgery
29d
Cleared
Oct 09, 2018
Senhance Surgical System
General & Plastic Surgery
123d
Cleared
May 25, 2018
TransEnterix Senhance Surgical System
General & Plastic Surgery
126d
Cleared
Oct 13, 2017
Senhance Surgical Robotic System
General & Plastic Surgery
182d
Cleared
Oct 25, 2012
SPIDER SURGICAL INSTRUMENTS, FLEXIBLE MONOPOLAR GRASPER WAVY RATCHETED,...
General & Plastic Surgery
86d
Cleared
Apr 16, 2012
SPIDER FLEXIBLE BLUNT DISSECTOR AND BAND PASSER
General & Plastic Surgery
67d
Cleared
Mar 15, 2011
SPIDER STANDARD AND ADVANCED
General & Plastic Surgery
167d