Visionsense, Ltd.
Visionsense, Ltd. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2022, with 3 FDA device recalls on record.
Top product codes for Visionsense, Ltd.
FDA recalls by Visionsense, Ltd.
- Z-0280-2023 — VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012
- Z-0282-2023 — VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001
- Z-0281-2023 — VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS) - 785nm Product Number: 175-0012
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Visionsense, Ltd.
- K223020 — VS3-Iridium System (VS3-IR)
- K210265 — VS3 Iridium Sytem
- K171208 — Trans-anal Introducer
- K153548 — VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
- K152204 — VS3-IR system
- K150018 — VS3-IR-MMS System
- K141002 — VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
- K131434 — VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
- K123467 — VS3
- K082355 — VISIONSENSE STEREOSCOPIC VISION SYSTEM
- K082667 — VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)
- K081102 — VSU - VISIONSENSE STEREOSCOPIC VISION SYSTEM
- K073279 — VS-VISIONSENSE STEREOSCOPIC VISION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.