Neotract, Inc. - FDA 510(k) Cleared Devices
17
Total
16
Cleared
1
Denied
FDA 510(k) cleared devices by Neotract, Inc. Gastroenterology & Urology ✕
11 devices
Cleared
Sep 22, 2023
UroLift 2 ATC Advanced Tissue Control System
Gastroenterology & Urology
30d
Cleared
Jul 31, 2020
UroLift 2 System (formerly UL500), UroLift 2 Delivery Handle, UroLift 2...
Gastroenterology & Urology
29d
Cleared
Jun 05, 2020
UroLift Advanced Tissue Control (ATC) System
Gastroenterology & Urology
102d
Cleared
Dec 20, 2019
UroLift System (UL400)
Gastroenterology & Urology
24d
Cleared
Mar 21, 2019
UroLift System UL400
Gastroenterology & Urology
30d
Cleared
Dec 28, 2017
UroLift System (UL400 and UL500)
Gastroenterology & Urology
90d
Cleared
Aug 18, 2017
UroLift System (UL500)
Gastroenterology & Urology
14d
Cleared
Sep 21, 2016
UroLift System UL500, UroLift Delivery Handle, UroLift Implant Cartiridge
Gastroenterology & Urology
30d
Cleared
Mar 15, 2016
NeoTract UroLift System UL500
Gastroenterology & Urology
91d
Cleared
Dec 20, 2013
NEOTRACT UROLIFT SYSTEM
Gastroenterology & Urology
56d
Not Cleared
Sep 13, 2013
UROLIFT SYSTEM
Gastroenterology & Urology
190d