V.S.S.I., Inc.
Country not established
- Devices
- 1
What V.S.S.I., Inc. makes
V.S.S.I., Inc. manufactures the SER-TEX, a medical device designed for surgical or procedural use, though specific applications are not detailed.
The SER-TEX is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Ser-Tex Ref K800834
510(k) 510(k)
Frequently asked questions
How many devices does V.S.S.I., Inc. have in the registry?
The registry currently lists 1 device for V.S.S.I., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list V.S.S.I., Inc.'s devices?
Among its 1 most recently registered device, V.S.S.I., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do V.S.S.I., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for V.S.S.I., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from V.S.S.I., Inc. in the registry?
The most recently registered devices listed for V.S.S.I., Inc. include SER-TEX.