Innovative Therapies, Inc. is one of 23486 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Innovative Therapies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANTLIA III WOUND TREATMENT SYSTEM, SVED WOUND TREATMENT SYSTEM, ANTLIA I WOUND IRRIGATION SYSTEM
4
Total
4
Cleared
0
Denied
Innovative Therapies, Inc. has 4 FDA 510(k) cleared medical devices. Based in Simpsonville, US.
Historical record: 4 cleared submissions from 2007 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Innovative Therapies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Innovative Therapies, Inc.
4 devices
Cleared
Aug 08, 2011
ANTLIA III WOUND TREATMENT SYSTEM
General & Plastic Surgery
88d
Cleared
Nov 25, 2009
SVED WOUND TREATMENT SYSTEM
General & Plastic Surgery
7d
Cleared
May 24, 2007
ANTLIA I WOUND IRRIGATION SYSTEM
General & Plastic Surgery
15d
Cleared
Apr 13, 2007
ANTLIA II SUCTION PUMP SYSTEM
General & Plastic Surgery
11d