Medical Device Manufacturer · US , Washington , DC

Visionsense, Ltd. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2008

Recent clearances: VS3-Iridium System (VS3-IR), VS3 Iridium Sytem, Trans-anal Introducer

13

Total

13

Cleared

0

Denied

FDA 510(k) Regulatory Record - Visionsense, Ltd. General & Plastic Surgery ✕

6 devices

1-6 of 6

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 Oct 28, 2015

General & Plastic Surgery · 83d

Cleared Jun 17, 2015

VS3-IR-MMS System

General & Plastic Surgery · 163d

Cleared Apr 17, 2013

General & Plastic Surgery · 159d

Cleared Mar 05, 2008

VS-VISIONSENSE STEREOSCOPIC VISION SYSTEM

General & Plastic Surgery · 105d