Vertis Neuroscience, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Vertis Neuroscience, Inc. makes
Vertis Neuroscience, Inc. manufactures percutaneous nerve stimulation devices, including control units and safeguide guides for pediatric and cervical applications. The VERTIS PNT Control Unit (CU100) and VERTIS PNT Safeguide (pediatric and cervical models) are designed for nerve stimulation procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vertis Neuroscience, Inc. have in the registry?
The registry currently lists 2 devices for Vertis Neuroscience, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vertis Neuroscience, Inc.'s devices?
Among its 2 most recently registered devices, Vertis Neuroscience, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vertis Neuroscience, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vertis Neuroscience, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vertis Neuroscience, Inc. in the registry?
The most recently registered devices listed for Vertis Neuroscience, Inc. include VERTIS PNT CONTROL UNIT, VERTIS PNT SAFEGUIDE KIDS, MODELS CU100, SGXXX and VERTIS PNT CONTROL UNIT, MODEL CU 100; VERTIS PNT SAFEGUIDE-CERVICAL, MODEL SG 102-XXX.