Spinal Analytics & Geometrical Impant Co, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Spinal Analytics & Geometrical Impant Co, LLC makes
Spinal Analytics & Geometrical Implant Co, LLC manufactures interbody fusion systems for spinal surgery, including the ARIA Lumbar and ARION Cervical devices designed for lumbar and cervical spine stabilization.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
TotalTi ACDF by SAGICO Ref K233191
Regimes: 510(k) Registry: 510(k)SAGICO OSI Spinal System by Osimplant Ref K180220
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spinal Analytics & Geometrical Impant Co, LLC have in the registry?
The registry currently lists 3 devices for Spinal Analytics & Geometrical Impant Co, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinal Analytics & Geometrical Impant Co, LLC's devices?
Among its 3 most recently registered devices, Spinal Analytics & Geometrical Impant Co, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Spinal Analytics & Geometrical Impant Co, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Spinal Analytics & Geometrical Impant Co, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinal Analytics & Geometrical Impant Co, LLC in the registry?
The most recently registered devices listed for Spinal Analytics & Geometrical Impant Co, LLC include TotalTi ACDF by SAGICO, SAGICO OSI Spinal System by Osimplant and SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL.