Neuro Spinal Innovation, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Neuro Spinal Innovation, Inc. makes
Neuro Spinal Innovation, Inc. manufactures the SONIK MONARK 100, a device designed for spinal cord stimulation or neuromodulation applications.
The SONIK MONARK 100 is classified as a Class II (U) device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
Sonik Monark 100 Ref K234036
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 240376810
Frequently asked questions
How many devices does Neuro Spinal Innovation, Inc. have in the registry?
The registry currently lists 2 devices for Neuro Spinal Innovation, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuro Spinal Innovation, Inc.'s devices?
Among its 2 most recently registered devices, Neuro Spinal Innovation, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What are the newest devices from Neuro Spinal Innovation, Inc. in the registry?
The most recently registered devices listed for Neuro Spinal Innovation, Inc. include SONIK SM-100 and SONIK MONARK 100.