Visionsense, Ltd. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Visionsense, Ltd. has 13 FDA 510(k) cleared medical devices. Based in Washington, US.
Last cleared in 2022. Active since 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Visionsense, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Visionsense, Ltd.
13 devices
Cleared
Oct 28, 2022
VS3-Iridium System (VS3-IR)
General & Plastic Surgery
29d
Cleared
Nov 22, 2021
VS3 Iridium Sytem
General & Plastic Surgery
294d
Cleared
Feb 05, 2018
Trans-anal Introducer
Gastroenterology & Urology
286d
Cleared
Feb 22, 2016
VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
Orthopedic
73d
Cleared
Oct 28, 2015
VS3-IR system
General & Plastic Surgery
83d
Cleared
Jun 17, 2015
VS3-IR-MMS System
General & Plastic Surgery
163d
Cleared
Jun 26, 2014
VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
Orthopedic
69d
Cleared
Jul 16, 2013
VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
Neurology
60d
Cleared
Apr 17, 2013
VS3
General & Plastic Surgery
159d
Cleared
Dec 15, 2008
VISIONSENSE STEREOSCOPIC VISION SYSTEM
Orthopedic
122d
Cleared
Oct 30, 2008
VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)
Ear, Nose, Throat
48d
Cleared
May 29, 2008
VSU - VISIONSENSE STEREOSCOPIC VISION SYSTEM
Neurology
42d