Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013559620

FEI Number

3013559620

Entity Name

EOSERA INC

City/State/Country

Fort Worth, TX, US

Establishment Address

5000 South Freeway, Suite 106, Fort Worth, TX 76115, US

Establishment Type(s)

Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Eosera Inc (Owner Number: 10058317)

Owner / Operator Contact Address

5000 South Freeway, Suite 110, Fort Worth, TX 76115, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ear Irrigation Kit with irrigation bulb syringe Wax Blaster MD Ear Irrigation and Cleaning Kit with Ear Clean MD

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OGQ	Ear Irrigation Kit	General Hospital	Class 1	880.6960	2018-08-22

Official Correspondent

Pam Clark

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Eosera 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 3013559620. Last updated year: 2026. Please use registration number 3013559620 when referencing this establishment in official correspondence.