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Theranica Bio-Electronics, Ltd.

US

Last updated May 31, 2026

What Theranica Bio-Electronics, Ltd. makes

Theranica Bio-Electronics, Ltd. manufactures craniofacial analgesia electrical stimulators designed for pain management, including portable devices for migraine relief. Their portfolio includes rechargeable stimulators and disposable refill cartridges for extended use, all intended for non-invasive treatment of acute migraine attacks.

The company’s devices are classified as Class II under regulatory frameworks, with authorisations granted through FDA 510(k) and De Novo pathways. Products are listed in the FDA’s regulatory databases, and the manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
—
Website
nerivio.com
LinkedIn
—
Facebook
—
Phone
937-6374846
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
532352807

Catalogue (12)

DeviceModel / ReferenceRegistriesClassStatus
Nerivio FGD000075
FDA UDI
Class IIActive
Nerivio Infinity FGD000100
FDA UDI
Class IIActive
Nerivio FGD000075
FDA UDI
Class IIActive
Nerivio Infinity Refill FGD000110
FDA UDI
Class IIActive
Nerivio Infinity FGD000100
FDA UDI
Class IIActive
Nerivio; Nerivio Infinity K250405
FDA 510(k)
Class IIActive
Nerivio, FGD000075-4.7 K203181
FDA 510(k)
Class IIActive
Nerivio K223169
FDA 510(k)
Class IIActive
Nerivio K201824
FDA 510(k)
Class IIActive
NerivioInfinity K232152
FDA 510(k)
Class IIActive
Nerivio Migra DEN180059
FDA 510(k)
Class IIActive
Nerivio; NerivioInfinity K241756
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Theranica Bio-Electronics Ltd. Netanya Central · IL FEI 3015379717