Vinyl Technology, Inc.
Country not established FDA establishment FEI 2023711
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
What Vinyl Technology, Inc. makes
Vinyl Technology, Inc. manufactures inflatable splints and anti-shock garments, including inflatable half leg splints, inflatable foot and ankle splints, inflatable full leg splints, inflatable full arm splints, and pneumatic trousers with three bladders designed for anti-shock use.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Inflatable Half Leg Splint Ref K874052
510(k) 510(k)Trousers, Pneumatic, Anti-Shock Three Bladders Ref K874774
510(k) 510(k)Inflatable Foot & Ankle Splint Ref K874050
510(k) 510(k)Inflatable Full Leg Splint Ref K874051
510(k) 510(k)Inflatable Full Arm Splint Ref K874053
510(k) 510(k)
Company details
- FDA FEI number
- 2023711
- Address
- 200 RAILROAD AVE., MONROVIA, CA, 91016
Frequently asked questions
How many devices does VINYL TECHNOLOGY, INC. have in the registry?
The registry currently lists 5 devices for VINYL TECHNOLOGY, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VINYL TECHNOLOGY, INC.'s devices?
Among its 5 most recently registered devices, VINYL TECHNOLOGY, INC. has devices listed in FDA 510(k) (5 devices).
What risk classes do VINYL TECHNOLOGY, INC.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for VINYL TECHNOLOGY, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from VINYL TECHNOLOGY, INC. in the registry?
The most recently registered devices listed for VINYL TECHNOLOGY, INC. include INFLATABLE HALF LEG SPLINT, TROUSERS, PNEUMATIC, ANTI-SHOCK THREE BLADDERS, INFLATABLE FOOT & ANKLE SPLINT and INFLATABLE FULL LEG SPLINT.