Neurotrigger
IsraelFDA 510(k) applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Neurotrigger makes
Neurotrigger manufactures the NeuroTrigger Basic (NTB), a device designed for neuromodulation applications, likely targeting peripheral nerve stimulation or related therapeutic interventions.
The NeuroTrigger Basic (NTB) is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
NeuroTrigger Basic (NTB) Ref K223027
510(k) 510(k)
FDA establishments
- Neurotrigger Ltd US
Frequently asked questions
How many devices does Neurotrigger have in the registry?
The registry currently lists 1 device for Neurotrigger. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurotrigger's devices?
Among its 1 most recently registered device, Neurotrigger has devices listed in FDA 510(k) (1 device).
What risk classes do Neurotrigger's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurotrigger's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurotrigger in the registry?
The most recently registered devices listed for Neurotrigger include NeuroTrigger Basic (NTB).
Which FDA establishments are linked to Neurotrigger?
1 FDA establishment is linked to Neurotrigger in the registry; they are listed on the company page.