Surgical Technology Laboratories, Inc (Stl)
Country not established
- Devices
- 1
What Surgical Technology Laboratories, Inc (Stl) makes
Surgical Technology Laboratories, Inc (Stl) makes PUREFORM EPTFE facial implants for nasal, chin, and malar applications.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgical Technology Laboratories, Inc ("Stl") have in the registry?
The registry currently lists 1 device for Surgical Technology Laboratories, Inc ("Stl"). Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgical Technology Laboratories, Inc ("Stl")'s devices?
Among its 1 most recently registered device, Surgical Technology Laboratories, Inc ("Stl") has devices listed in FDA 510(k) (1 device).
What risk classes do Surgical Technology Laboratories, Inc ("Stl")'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgical Technology Laboratories, Inc ("Stl")'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgical Technology Laboratories, Inc ("Stl") in the registry?
The most recently registered devices listed for Surgical Technology Laboratories, Inc ("Stl") include PUREFORM EPTFE FACIAL IMPLANTS (NASAL, CHIN, MALER).