Diagnospine Fabrication, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Diagnospine Fabrication, Inc. makes
Diagnospine Fabrication, Inc. manufactures the Spinoscope, a device designed for spinal imaging and diagnostic procedures. This product is intended for use in visualizing spinal anatomy during surgical interventions or diagnostic evaluations.
The Spinoscope is classified as a Class II medical device under US regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Spinoscope Ref K872836
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnospine Fabrication, Inc. have in the registry?
The registry currently lists 1 device for Diagnospine Fabrication, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnospine Fabrication, Inc.'s devices?
Among its 1 most recently registered device, Diagnospine Fabrication, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Diagnospine Fabrication, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Diagnospine Fabrication, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnospine Fabrication, Inc. in the registry?
The most recently registered devices listed for Diagnospine Fabrication, Inc. include SPINOSCOPE.