Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012112259

FEI Number

3012112259

Entity Name

AVENTAMED DAC

City/State/Country

Bishopstown Cork, IE

Establishment Address

Rubicon Centre, Rossa Avenue, Bishopstown Cork T12Y275, IE

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

AventaMed DAC (Owner Number: 10091035)

Owner / Operator Contact Address

Rubicon Centre, Rossa Avenue, Bishopstown, IE-CR T12Y275, IE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K250256

PMA Number

N/A

All Registered Proprietary Names

Solo+ TTD

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ETD	Tube, Tympanostomy	Ear, Nose, Throat	Class 2	874.3880	2025-07-08

Official Correspondent

John Vaughan

US Agent Details

Anja Fair Business: KARL STORZ ENDOSCOPY-AMERICA, INC. Email: anja.fair@karlstorz.com Phone: (346) 8168200

Related Public Records

Same Entity

AventaMed DAC

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 3012112259. Last updated year: 2026. Please use registration number 3012112259 when referencing this establishment in official correspondence.