Biomet Trauma (Aka Ebi, LLC)
United StatesFDA applicant, unverified
- Devices
- 4
What Biomet Trauma (Aka Ebi, LLC) makes
Biomet Trauma (also known as Ebi, LLC) manufactures the MAC MALE ADAPTER, a medical device used in trauma applications.
The MAC MALE ADAPTER is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Smple Plate And Screws Ref K093983
Regimes: 510(k) Registry: 510(k)Biomet Forerunner Locking Plate System Ref K092528
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Mac Male Adapter Ref K102843
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomet Trauma (Aka Ebi, LLC) have in the registry?
The registry currently lists 4 devices for Biomet Trauma (Aka Ebi, LLC). Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomet Trauma (Aka Ebi, LLC)'s devices?
Among its 4 most recently registered devices, Biomet Trauma (Aka Ebi, LLC) has devices listed in FDA 510(k) (4 devices).
What risk classes do Biomet Trauma (Aka Ebi, LLC)'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Biomet Trauma (Aka Ebi, LLC)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomet Trauma (Aka Ebi, LLC) in the registry?
The most recently registered devices listed for Biomet Trauma (Aka Ebi, LLC) include SMPLE PLATE AND SCREWS, BIOMET FORERUNNER LOCKING PLATE SYSTEM, OPTILOCK VL (VARIABLE ANGLE LOCKING) DISTAL RADIUS PLATING SYSTEM and MAC MALE ADAPTER.