Tekka
Country not established
- Devices
- 2
What Tekka makes
Tekka makes the ORTRAUTEK Trauma System and the ORTRAUTEK Orthognathic System, which are medical devices used in surgical procedures involving bone fixation and jaw realignment.
These devices are classified as Class II and are listed in the FDA 510(k) registry; Tekka is based in the United States.
Catalogue
Ortrautek Trauma System Ref K032520
Regimes: 510(k) Registry: 510(k)Ortrautek Orthognathic System Ref K031989
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tekka have in the registry?
The registry currently lists 2 devices for Tekka. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tekka's devices?
Among its 2 most recently registered devices, Tekka has devices listed in FDA 510(k) (2 devices).
What risk classes do Tekka's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tekka's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tekka in the registry?
The most recently registered devices listed for Tekka include ORTRAUTEK TRAUMA SYSTEM and ORTRAUTEK ORTHOGNATHIC SYSTEM.