Pinpointe USA, Inc.
Country not established
- Devices
- 1
What Pinpointe USA, Inc. makes
Pinpointe USA, Inc. makes medical devices such as the PINPOINTE FOOTLASER.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pinpointe Footlaser Ref K093547
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pinpointe USA, Inc. have in the registry?
The registry currently lists 1 device for Pinpointe USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pinpointe USA, Inc.'s devices?
Among its 1 most recently registered device, Pinpointe USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pinpointe USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pinpointe USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pinpointe USA, Inc. in the registry?
The most recently registered devices listed for Pinpointe USA, Inc. include PINPOINTE FOOTLASER.