Porex Surgical Products Group
Country not established
- Devices
- 1
What Porex Surgical Products Group makes
Porex Surgical Products Group manufactures the MEDPOR PTERIONAL SURGICAL IMPLANT, a porous polyethylene device designed for cranial reconstruction and bone regeneration in surgical applications.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Medpor Pterional Surgical Implant Ref K002586
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Porex Surgical Products Group have in the registry?
The registry currently lists 1 device for Porex Surgical Products Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Porex Surgical Products Group's devices?
Among its 1 most recently registered device, Porex Surgical Products Group has devices listed in FDA 510(k) (1 device).
What risk classes do Porex Surgical Products Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Porex Surgical Products Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Porex Surgical Products Group in the registry?
The most recently registered devices listed for Porex Surgical Products Group include MEDPOR PTERIONAL SURGICAL IMPLANT.