Tekno-Medical
Country not established
- Devices
- 1
What Tekno-Medical makes
Tekno-Medical manufactures bone screws designed specifically for maxillofacial applications, used in surgical procedures involving the jaw and facial bones.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Screw, Bone, Maxillofacial Ref K911165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tekno-Medical have in the registry?
The registry currently lists 1 device for Tekno-Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tekno-Medical's devices?
Among its 1 most recently registered device, Tekno-Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Tekno-Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tekno-Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tekno-Medical in the registry?
The most recently registered devices listed for Tekno-Medical include SCREW, BONE, MAXILLOFACIAL.