Raed M. Ali, M.D., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Raed M. Ali, M.D., Inc. makes
Raed M. Ali, M.D., Inc. manufactures the Ali Interbody Fusion System, a spinal interbody device designed for intervertebral fusion procedures in the lumbar spine. The system is intended for use in anterior lumbar interbody fusion (ALIF) and lateral lumbar interbody fusion (LLIF) surgeries to stabilize the spine and promote bone growth between vertebrae.
The Ali Interbody Fusion System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Ali Interbody Fusion System Ref K191516
Regimes: 510(k) Registry: 510(k)Ali Interbody Fusion System Ref K203308
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Raed M. Ali, M.D., Inc. have in the registry?
The registry currently lists 2 devices for Raed M. Ali, M.D., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Raed M. Ali, M.D., Inc.'s devices?
Among its 2 most recently registered devices, Raed M. Ali, M.D., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Raed M. Ali, M.D., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Raed M. Ali, M.D., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Raed M. Ali, M.D., Inc. in the registry?
The most recently registered devices listed for Raed M. Ali, M.D., Inc. include Ali Interbody Fusion System.