Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Theralight, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K061295	VERSACLEAR SKIN THERAPY SYSTEM, MODEL 100	FTC	2006-05-25	View
510(k)	K051259	VERSACLEAR SKIN THERAPY SYSTEM, MODEL 100	GEX	2005-09-20	View
510(k)	K024020	THERALIGHT UV120-2 UVA/UVB PHOTOTHERAPY SYSTEM	FTC	2003-01-17	View
510(k)	K022165	THERALIGHT UV120-2 UVA/UVB PHOTOTHERAPY SYSTEM, MODEL UV120-2	FTC	2002-07-18	View

↑