Orthopaedic & Spine Development
FranceFDA 510(k) applicant, unverified
- Devices
- 19
Catalogue
Search and filter all 19 devicesCompany details
- DUNS number
- 282063846
- [email protected]
- Phone
- +330432740110
Frequently asked questions
How many devices does ORTHOPAEDIC & SPINE DEVELOPMENT have in the registry?
The registry currently lists 19 devices for ORTHOPAEDIC & SPINE DEVELOPMENT. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORTHOPAEDIC & SPINE DEVELOPMENT's devices?
Among its 19 most recently registered devices, ORTHOPAEDIC & SPINE DEVELOPMENT has devices listed in FDA 510(k) (1 device) and FDA GUDID (18 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ORTHOPAEDIC & SPINE DEVELOPMENT's devices fall under?
Among its 19 most recently registered devices, the classes recorded for ORTHOPAEDIC & SPINE DEVELOPMENT's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ORTHOPAEDIC & SPINE DEVELOPMENT in the registry?
The most recently registered devices listed for ORTHOPAEDIC & SPINE DEVELOPMENT include Orthopaedic & Spine Development (OSD) VREV-0017, Orthopaedic & Spine Development (OSD) A-CPL-0002, Orthopaedic & Spine Development (OSD) PCEV-0026 and Orthopaedic & Spine Development (OSD) VREV-0013.