Mylad Orthopedic Solutions, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Mylad Orthopedic Solutions, LLC makes
Mylad Orthopedic Solutions, LLC makes the Olecranail Intramedullary Fixation System, a device used for stabilizing fractures of the olecranon process of the ulna.
The Olecranail Intramedullary Fixation System is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Olecra Intramedullary Fixation System Ref K110322
Regimes: 510(k) Registry: 510(k)Olecranail Intramedullary Fixation System Ref K081356
Regimes: 510(k) Registry: 510(k)Olecranail Intramedullary Fixation System Ref K090091
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mylad Orthopedic Solutions, LLC have in the registry?
The registry currently lists 3 devices for Mylad Orthopedic Solutions, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mylad Orthopedic Solutions, LLC's devices?
Among its 3 most recently registered devices, Mylad Orthopedic Solutions, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Mylad Orthopedic Solutions, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mylad Orthopedic Solutions, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mylad Orthopedic Solutions, LLC in the registry?
The most recently registered devices listed for Mylad Orthopedic Solutions, LLC include OLECRA INTRAMEDULLARY FIXATION SYSTEM and OLECRANAIL INTRAMEDULLARY FIXATION SYSTEM.