Glasir Medical LP
Country not established
- Devices
- 31
What Glasir Medical LP makes
Glasir Medical LP manufactures polymeric spinal interbody fusion cages, including PEEK-based implants for cervical and posterior lumbar interbody fusion (PLIF). These devices are designed for spinal stabilization and fusion procedures in the cervical and lumbar regions.
The company’s products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. Glasir Medical LP is based in the United States.
Catalogue
Search and filter all 31 devicesCompany details
- DUNS number
- 066151033
Frequently asked questions
How many devices does GLASIR MEDICAL LP have in the registry?
The registry currently lists 31 devices for GLASIR MEDICAL LP. Devices recorded under merged duplicate company entries are counted once.
Which registries list GLASIR MEDICAL LP's devices?
Among its 31 most recently registered devices, GLASIR MEDICAL LP has devices listed in FDA GUDID (31 devices).
What risk classes do GLASIR MEDICAL LP's devices fall under?
Among its 31 most recently registered devices, the classes recorded for GLASIR MEDICAL LP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from GLASIR MEDICAL LP in the registry?
The most recently registered devices listed for GLASIR MEDICAL LP include Emerald Cervical PEEK C-P-035, Emerald Cervical PEEK C-P-032, Emerald Cervical PEEK C-L-037 and Emerald Cervical PEEK C-L-031.