Vitage Led, Ltd. is one of 462 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Vitage Led, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LIGHTFUSION LED SYSTEM
1
Total
1
Cleared
0
Denied
Vitage Led, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Basildon, GB.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vitage Led, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ismart Marketing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Vitage Led, Ltd.
1 devices