Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002224346

FEI Number

3002224346

Entity Name

AJL OPHTHALMIC, S.A.

City/State/Country

MINANO Alava, ES

Establishment Address

FERDINAND ZEPPELIN, 1, PARQUE TECNOLOGICO ALAVA, MINANO Alava 01510, ES

Establishment Type(s)

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

Owner / Operator

AJL OPHTHALMIC, S.A. (Owner Number: 9104919)

Owner / Operator Contact Address

FERDINAND ZEPPELIN, 1, PARQUE TECNOLOGICO ALAVA, MIÑANO, ES-PV 01510, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Vacuum Centering Guide VAMA AIRWAY CANNULA VAMA

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HNH	Ring, Ophthalmic (Flieringa)	Ophthalmic	Class 1	886.4350	2026-03-11
CAE	Airway, Oropharyngeal, Anesthesiology	Anesthesiology	Class 1	868.5110	2007-07-26

Official Correspondent

EVA LARRA

US Agent Details

Daniel Salazar Business: Addition Technology Inc Email: dsalazar@additiontechnology.com Phone: (847) 2978419

Related Public Records

Same Entity

AJL OPHTHALMIC, S.A.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2014	King Systems Corp.	1	King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

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3030451558	BIS MASTERMED	Kosice Kosicky, SK
3003951061	M/S TARUN ENTERPRISES	Prayagraj, Uttar Pradesh, IN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002224346. Last updated year: 2026. Please use registration number 3002224346 when referencing this establishment in official correspondence.