Biomet Spine (Aka Ebi, LLC)
United StatesFDA applicant, unverified
- Devices
- 14
What Biomet Spine (Aka Ebi, LLC) makes
Biomet Spine (Aka Ebi, LLC) manufactures spinal fixation and interbody devices, including the Polaris Spinal System, Gallery Laminoplasty Fixation System, Maxan Anterior Cervical Plate System, and Zyston Arc Interbody Spacer. The company also produces related instrumentation such as the Polaris Spinal System - Ballista II Percutaneous Screw Placement System, Polaris Spinal System - Ballista II Rods, Biomet Access System, Biomet Graft Delivery Syringes, and Biomet Lateral Spacer System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 14 devicesFrequently asked questions
How many devices does Biomet Spine (Aka Ebi, LLC) have in the registry?
The registry currently lists 14 devices for Biomet Spine (Aka Ebi, LLC). Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomet Spine (Aka Ebi, LLC)'s devices?
Among its 14 most recently registered devices, Biomet Spine (Aka Ebi, LLC) has devices listed in FDA 510(k) (14 devices).
What risk classes do Biomet Spine (Aka Ebi, LLC)'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Biomet Spine (Aka Ebi, LLC)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomet Spine (Aka Ebi, LLC) in the registry?
The most recently registered devices listed for Biomet Spine (Aka Ebi, LLC) include POLARIS SPINAL SYSTEM, NEXTGEN ALTIUS OCT SYSTEM, ZYSTON ARC INTERBODY SPACER and GALLERY LAMINOPLASTY FIXATION SYSTEM.