Arnell, Inc.
Country not established
- Devices
- 1
What Arnell, Inc. makes
Arnell, Inc. makes the Rabinowitz Gum Massager, a device intended for oral care and gum stimulation.
The Rabinowitz Gum Massager is classified as a Class I medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Rabinowitz Gum Massager Ref K862635
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arnell, Inc. have in the registry?
The registry currently lists 1 device for Arnell, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arnell, Inc.'s devices?
Among its 1 most recently registered device, Arnell, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Arnell, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Arnell, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Arnell, Inc. in the registry?
The most recently registered devices listed for Arnell, Inc. include RABINOWITZ GUM MASSAGER.