Neurotechnics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Neurotechnics, Inc. makes
Neurotechnics, Inc. manufactures needle electrodes designed for medical procedures, including low-profile and high-profile variants for precise neural stimulation or recording applications.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Low Profile Needle Electrode (N-Spyral LP) Ref K863135
Regimes: 510(k) Registry: 510(k)High Profile Needle Electrode (N-Spyral Hp) Ref K863136
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurotechnics, Inc. have in the registry?
The registry currently lists 2 devices for Neurotechnics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurotechnics, Inc.'s devices?
Among its 2 most recently registered devices, Neurotechnics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Neurotechnics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neurotechnics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurotechnics, Inc. in the registry?
The most recently registered devices listed for Neurotechnics, Inc. include LOW PROFILE NEEDLE ELECTRODE (N-SPYRAL LP) and HIGH PROFILE NEEDLE ELECTRODE (N-SPYRAL HP).