Globus Industries
Country not established
- Devices
- 1
What Globus Industries makes
Globus Industries manufactures the IM512P, a medical device designed for spinal surgical procedures, including interbody fusion applications. This product is intended for use in the lumbar and thoracic regions of the spine, providing structural support and facilitating bone fusion.
The IM512P is classified under Class I by the FDA and has undergone 510(k) clearance. The company operates within the United States, adhering to regulatory standards for spinal implants and surgical devices.
Catalogue
IM512P Ref K945792
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Globus Industries have in the registry?
The registry currently lists 1 device for Globus Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Globus Industries's devices?
Among its 1 most recently registered device, Globus Industries has devices listed in FDA 510(k) (1 device).
What risk classes do Globus Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for Globus Industries's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Globus Industries in the registry?
The most recently registered devices listed for Globus Industries include IM512P.