Theralight, Inc. is one of 23657 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theralight, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VERSACLEAR SKIN THERAPY SYSTEM, MODEL 100, VERSACLEAR SKIN THERAPY SYSTEM, MODEL 100, THERALIGHT UV120-2 UVA/UVB PHOTOTHERAPY SYSTEM
4
Total
4
Cleared
0
Denied
Theralight, Inc. has 4 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 4 cleared submissions from 2002 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Theralight, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Theralight, Inc.
4 devices
Cleared
May 25, 2006
VERSACLEAR SKIN THERAPY SYSTEM, MODEL 100
General & Plastic Surgery
16d
Cleared
Sep 20, 2005
VERSACLEAR SKIN THERAPY SYSTEM, MODEL 100
General & Plastic Surgery
127d
Cleared
Jan 17, 2003
THERALIGHT UV120-2 UVA/UVB PHOTOTHERAPY SYSTEM
General & Plastic Surgery
43d
Cleared
Jul 18, 2002
THERALIGHT UV120-2 UVA/UVB PHOTOTHERAPY SYSTEM, MODEL UV120-2
General & Plastic Surgery
15d