Akros Medical
Country not established
- Devices
- 3
What Akros Medical makes
Akros Medical manufactures orthopedic repair kits, including the Akros FibuLink™ Syndesmosis Repair Kit, the Akros Fibulink Syndesmosis Repair Kit, and the Akros Suture Anchor LisFranc Repair Kit, which are used for ligament and bone fixation procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. Akros Medical is based in the United States.
Catalogue
Akros FibuLink™ Syndesmosis Repair Kit Ref K173550
Regimes: 510(k) Registry: 510(k)Akros Fibulink Syndesmosis Repair Kit Ref K162805
Regimes: 510(k) Registry: 510(k)Akros Scruture Anchor LisFranc Repair Kit Ref K200361
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Akros Medical have in the registry?
The registry currently lists 3 devices for Akros Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Akros Medical's devices?
Among its 3 most recently registered devices, Akros Medical has devices listed in FDA 510(k) (3 devices).
What risk classes do Akros Medical's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Akros Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Akros Medical in the registry?
The most recently registered devices listed for Akros Medical include Akros FibuLink™ Syndesmosis Repair Kit, Akros Fibulink Syndesmosis Repair Kit and Akros Scruture Anchor LisFranc Repair Kit.