Lynton Lasers Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Lynton Lasers Limited - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Lynton Lasers Limited has 3 FDA 510(k) cleared medical devices. Based in Holmes Chapel, Cheshire, GB.
Historical record: 3 cleared submissions from 2006 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lynton Lasers Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lynton Lasers Limited
3 devices
Cleared
Nov 16, 2007
LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC...
Physical Medicine
114d
Cleared
Jul 25, 2007
LUMINA INTENSE PULSED LIGHT (& LASER) SYSTEM
General & Plastic Surgery
254d
Cleared
Nov 14, 2006
LUMACARE LC-122M NON-COHERENT LIGHT SOURCE
General & Plastic Surgery
50d