Archimed, Inc.
Country not established
- Devices
- 1
What Archimed, Inc. makes
Archimed, Inc. manufactures the ARCHIMED REMEDY CERVICAL PLATE, a spinal fixation device designed for cervical spine stabilization procedures.
The company’s portfolio is regulated under FDA Class II devices, with the ARCHIMED REMEDY CERVICAL PLATE listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Archimed Remedy Cervical Plate Ref K100215
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Archimed, Inc. have in the registry?
The registry currently lists 1 device for Archimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Archimed, Inc.'s devices?
Among its 1 most recently registered device, Archimed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Archimed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Archimed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Archimed, Inc. in the registry?
The most recently registered devices listed for Archimed, Inc. include ARCHIMED REMEDY CERVICAL PLATE.