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
FDA 510(k) Regulatory Record - Theralight, Inc. General & Plastic Surgery ✕
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