Surgisil
Country not established
- Devices
- 1
What Surgisil makes
Surgisil manufactures PERMA Facial Implants, a permanent facial augmentation device designed for subcutaneous placement to enhance facial contours.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) premarket notifications. The manufacturer is based in the United States.
Catalogue
Perma Facial Implants Ref K071823
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgisil have in the registry?
The registry currently lists 1 device for Surgisil. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgisil's devices?
Among its 1 most recently registered device, Surgisil has devices listed in FDA 510(k) (1 device).
What risk classes do Surgisil's devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgisil's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgisil in the registry?
The most recently registered devices listed for Surgisil include PERMA FACIAL IMPLANTS.