Pain Prevention, Inc.
Country not established
- Devices
- 1
What Pain Prevention, Inc. makes
Pain Prevention, Inc. manufactures dental anesthesia apparatus designed for administering local anesthetics in clinical settings, including intraoral and periapical injections.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The apparatus is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Dental Anesthesia Apparatus Ref K850425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pain Prevention, Inc. have in the registry?
The registry currently lists 1 device for Pain Prevention, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pain Prevention, Inc.'s devices?
Among its 1 most recently registered device, Pain Prevention, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pain Prevention, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pain Prevention, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pain Prevention, Inc. in the registry?
The most recently registered devices listed for Pain Prevention, Inc. include DENTAL ANESTHESIA APPARATUS.