ElectroCore, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000036987 FEI 3015529603
ElectroCore, Inc. is a medical device manufacturer based in the United States, with 122 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II; EU Class IIa and I) as of 15 Nov 2026.
- Devices
- 122
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 86
- EUDAMED 36
- FDA 510(k) 3
- Device classes
- FDA Class II 89
- EU Class IIa 30
- EU Class I 3
- Top EMDN categories
- Sites and related companies
- MDSS GmbH authorised representative
- Identifiers
- EUDAMED SRN US-MF-000036987
- FDA FEI 3015529603
- DUNS 831341628
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- MDSS GmbHDE
What ElectroCore, Inc. makes
ElectroCore, Inc. manufactures peripheral nerve electrical stimulators for migraine therapy, including rechargeable and disposable devices designed for non-invasive treatment. The company also produces a point aesthesiometer for sensory testing. Replacement parts and demo kits for these devices are also part of the portfolio.
The portfolio includes devices classified as Class I, Class II, and Class IIa under regulatory frameworks. These products are listed in the EU’s eudamed database and the FDA’s Unique Device Identifier (UDI) system. The company is based in the United States.
Catalogue
Search and filter all 122 devicesShowing 1-50 of 122
Company details
- EUDAMED SRN
- US-MF-000036987
- SRN (system / procedure pack)
- US-PR-000049586
- FDA FEI number
- 3015529603
- DUNS number
- 831341628
- EUDAMED status
- Active
- EUDAMED registered name
- ElectroCore, Inc.
- EUDAMED abbreviated name
- ElectroCore
- Registered address
- 200, Forge Way, 07866, Rockaway, United States
- Website
- www.electrocore.com
- info@electrocore.com
- Phone
- +1-973-290-0097
- PRRC contact
- Leanne Usa
Frequently asked questions
How many devices does ElectroCore, Inc. have in the registry?
The registry currently lists 122 devices for ElectroCore, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ElectroCore, Inc.'s devices?
Among its 50 most recently registered devices, ElectroCore, Inc. has devices listed in EUDAMED (12 devices) and FDA GUDID (41 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ElectroCore, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for ElectroCore, Inc.'s devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from ElectroCore, Inc. in the registry?
The most recently registered devices listed for ElectroCore, Inc. include gammaCore Sapphire SLC Refill Card Kit, 93 days, gammaCore Sapphire SLC - Evaluation Refill Card Kit, gammaCore Sapphire 6-Month Evaluation Device Kit and gammaCore Sapphire 20016-00301-RPL.