Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3026616094

FEI Number

3026616094

Entity Name

NEURAMEDICA INC.

City/State/Country

Oregon City, OR, US

Establishment Address

1515 7th St STE A, Oregon City, OR 97045, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

NeuraMedica Inc. (Owner Number: 10087505)

Owner / Operator Contact Address

1515 7th St STE A, Oregon City, OR 97045, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K213813

PMA Number

N/A

All Registered Proprietary Names

DuraFuse

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FZP	Clip, Implantable	General, Plastic Surgery	Class 2	878.4300	2023-03-07

Official Correspondent

Rachel Dreilinger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NeuraMedica 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 3026616094. Last updated year: 2026. Please use registration number 3026616094 when referencing this establishment in official correspondence.