Vinyl Technology, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Vinyl Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in So. El Monte, US.
Historical record: 5 cleared submissions from 1987 to 1988. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vinyl Technology, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Feb 08, 1988
TROUSERS, PNEUMATIC, ANTI-SHOCK THREE BLADDERS
Anesthesiology
81d
Cleared
Nov 23, 1987
INFLATABLE FOOT & ANKLE SPLINT
General & Plastic Surgery
49d
Cleared
Nov 23, 1987
INFLATABLE FULL LEG SPLINT
General & Plastic Surgery
49d
Cleared
Nov 23, 1987
INFLATABLE HALF LEG SPLINT
General & Plastic Surgery
49d
Cleared
Nov 23, 1987
INFLATABLE FULL ARM SPLINT
General & Plastic Surgery
49d