Vts, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vts, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Vts, Inc. has 5 FDA 510(k) cleared medical devices. Based in Newkirk, US.
Historical record: 5 cleared submissions from 1999 to 2001. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Vts, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vts, Inc.
5 devices
Cleared
Nov 09, 2001
VT-1
Gastroenterology & Urology
88d
Cleared
Nov 09, 2001
SE-200
Gastroenterology & Urology
88d
Cleared
Nov 09, 2001
SE-300 VACUUM THERAPY SYSTEM
Gastroenterology & Urology
88d
Cleared
Nov 09, 2001
SE-100 VACUUM ERECTION DEVICE
Gastroenterology & Urology
88d
Cleared
Oct 05, 1999
V.T.S., INC. (V.T.-3)
Gastroenterology & Urology
75d