eNeura Inc

FDA Device Registration & Listing · Baltimore, MD, US · Registration 3008487930

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008487930
FEI Number
3008487930
Entity Name
eNeura Inc
City/State/Country
Baltimore, MD, US
Establishment Address
101 West Dickman St., Suite 900, Baltimore, MD 21230, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
eNeura Inc. (Owner Number: 10039355)
Owner / Operator Contact Address
225 Southern Blvd, Suite 202, West Palm Beach, FL 33405, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230358
PMA Number
N/A

All Registered Proprietary Names

eNeura Spring TMS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OKP Transcranial Magnetic Stimulator For The Treatment Of Migraine Headache Neurology Class 2 882.5808 2023-11-02

Official Correspondent

Teresa Kazaros

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

eNeura Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008487930. Last updated year: 2026. Please use registration number 3008487930 when referencing this establishment in official correspondence.
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