Nanolite Technology, Inc. is one of 23669 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nanolite Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NANOLITE SKIN CARE SYSTEM
1
Total
1
Cleared
0
Denied
Nanolite Technology, Inc. has 1 FDA 510(k) cleared medical devices. Based in Torrance, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Nanolite Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Nanolite Technology, Inc.
1 devices