OECHSLER MEXICO S.A. DE C.V.

FDA Device Registration & Listing · Santiago de Queretaro, MX · Registration 3032912822

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
3032912822
FEI Number
3032912822
Entity Name
OECHSLER MEXICO S.A. DE C.V.
City/State/Country
Santiago de Queretaro, MX
Establishment Address
Carretera Estatal 431, km 2+200, Interior 58, Hacienda La Machorra, Parque Tecnologico Innovacion, Santiago de Queretaro 76246, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Oechsler Mexico S.A. De C.V. (Owner Number: 10091697)
Owner / Operator Contact Address
Carretera Estatal 431, km 2+200, Interior 58, Hacienda La Machorra, Parque Tecnologico Innovacion, Santiago de Queretaro, MX-QUE 76246, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

McMurray

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2024-10-24

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp. Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Oechsler Mexico S.A. De C.V.
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.

Similar Registrations

Registration Number Establishment Name Location
3037007211 ARETE MEDICAL DEVICES Mullica Hill, NJ, US
3012508471 P3 MEDICAL LTD Bristol Bristol, City of, GB
3014829416 MCMURRAY MEDICAL Minneapolis, MN, US
3015314035 Bio-Med Healthcare Products Pvt. Ltd. Palwal Haryana, IN
3008281139 DANYANG XINYA VALVE CO., LTD. Danyang Jiangsu, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032912822. Last updated year: 2026. Please use registration number 3032912822 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.