Mortise Medical, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Mortise Medical, LLC makes
Mortise Medical, LLC manufactures the SyndesMetrics Syndesmosis Repair System, a device designed for internal fixation of syndesmotic ankle injuries, and LigaMetrics Suture Anchors, which are used for soft tissue attachment in orthopedic procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. Mortise Medical, LLC is based in the United States.
Catalogue
SyndesMetrics Syndesmosis Repair System Ref K172620
Regimes: 510(k) Registry: 510(k)LigaMetrics Suture Anchors Ref K171964
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mortise Medical, LLC have in the registry?
The registry currently lists 2 devices for Mortise Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mortise Medical, LLC's devices?
Among its 2 most recently registered devices, Mortise Medical, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Mortise Medical, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mortise Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mortise Medical, LLC in the registry?
The most recently registered devices listed for Mortise Medical, LLC include SyndesMetrics Syndesmosis Repair System and LigaMetrics Suture Anchors.