Perioseal
Country not established
- Devices
- 1
What Perioseal makes
Perioseal manufactures dental implants designed for osseointegration in oral and maxillofacial applications, intended to replace missing teeth and restore function.
The company’s portfolio is regulated as Class II medical devices under FDA 510(k) clearance requirements. Products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
The Perioseal Dental Implant Ref K965032
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perioseal have in the registry?
The registry currently lists 1 device for Perioseal. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perioseal's devices?
Among its 1 most recently registered device, Perioseal has devices listed in FDA 510(k) (1 device).
What risk classes do Perioseal's devices fall under?
Among its 1 most recently registered device, the classes recorded for Perioseal's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perioseal in the registry?
The most recently registered devices listed for Perioseal include THE PERIOSEAL DENTAL IMPLANT.