Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022777869

FEI Number

3022777869

Entity Name

Javid de Mexico S. De R.L. De C.V. (resplabs)

City/State/Country

Nogales Sonora, MX

Establishment Address

Blvd. Luis Donaldo Colosio 2880-D, Parque Industrial de Nogales, Nogales Sonora 84094, MX

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RespLabs Medical USA Inc. (Owner Number: 10060973)

Owner / Operator Contact Address

2015 N Forbes Blvd, Ste 101, Tucson, AZ 85745, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CPAP Mask Wipes

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BTI	Compressor, Air, Portable	Anesthesiology	Class 2	868.6250	2019-09-20
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2024-05-20
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2020-02-27
EPE	Brush, Cleaning, Tracheal Tube	Anesthesiology	Class 1	868.5795	2021-08-16
EFT	Cleanser, Denture, Over The Counter	Dental	Class 1	872.3520	2024-01-28

Official Correspondent

Brady Nelson

US Agent Details

Erissa Limketee Business: resplabs medical USA inc. Email: elim@resplabs.com Phone: (520) 6610822

Related Public Records

Same Entity

RespLabs Medical USA Inc.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3014624980	RESPLABS MEDICAL USA INC.	Tucson, AZ, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K900686	Medical Industries America, Inc.	MAXI COMPRESSORS	1990-04-26
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

Similar Registrations

Registration Number	Establishment Name	Location
3003803075	EMG TECHNOLOGY CO., LTD.	Taichung City, TW
3008496560	NINGBO GREETMED MEDICAL INSTRUMENTS CO., LTD.	Ningbo Zhejiang, CN
3007238566	BEIJING AEONMED CO., LTD.	Sanhe Hebei, CN
3012336822	GUANGDONG JINME MEDICAL TECHNOLOGY CO., LTD.	Foshan Guangdong, CN
2515872	DeVilbiss Healthcare LLC.	SOMERSET, PA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022777869. Last updated year: 2026. Please use registration number 3022777869 when referencing this establishment in official correspondence.