Restore Medical, Inc.
Country not established
- Devices
- 1
What Restore Medical, Inc. makes
Restore Medical, Inc. manufactures the Pillar Palatal Implant System, a device designed for soft tissue augmentation in the palate to improve snoring and mild obstructive sleep apnea by creating structural support.
The Pillar Palatal Implant System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Pillar Palatal Implant System Ref K040417
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Restore Medical, Inc. have in the registry?
The registry currently lists 1 device for Restore Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Restore Medical, Inc.'s devices?
Among its 1 most recently registered device, Restore Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Restore Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Restore Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Restore Medical, Inc. in the registry?
The most recently registered devices listed for Restore Medical, Inc. include PILLAR PALATAL IMPLANT SYSTEM.