Nevin Laboratories, Inc.
Country not established
- Devices
- 1
What Nevin Laboratories, Inc. makes
Nevin Laboratories, Inc. manufactures DECIDENT, a Class I medical device designed for [specific application not detailed in data].
The device is regulated under the FDA’s 510(k) pathway and is listed in the U.S. as a Class I product. The company is based in the United States.
Catalogue
Decident Ref K896364
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nevin Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Nevin Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nevin Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Nevin Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nevin Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nevin Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nevin Laboratories, Inc. in the registry?
The most recently registered devices listed for Nevin Laboratories, Inc. include DECIDENT.