Mobarn Medical Devices, LLC
Country not established
- Devices
- 1
What Mobarn Medical Devices, LLC makes
Mobarn Medical Devices, LLC makes spinal fusion systems, including posterior, transforaminal, direct lateral, and anterior lumbar interbody fusion cages.
The company's portfolio is classified as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mobarn Medical Devices, LLC have in the registry?
The registry currently lists 1 device for Mobarn Medical Devices, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mobarn Medical Devices, LLC's devices?
Among its 1 most recently registered device, Mobarn Medical Devices, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Mobarn Medical Devices, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mobarn Medical Devices, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mobarn Medical Devices, LLC in the registry?
The most recently registered devices listed for Mobarn Medical Devices, LLC include Mobarn 80:20 Lumbar Interbody Fusion System (Posterior Lumbar Interbody Fusion Cage (PLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Transforaminal Lumbar Interbody Fusion Cage (TLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Direct Lateral Lumbar Interbody Fusion Cage (DLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Anterior Lumbar Interbody Fusion Cage (ALIF)).