Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010790521

FEI Number

3010790521

Entity Name

Brady Mexico, S. de R.L. de C.V.

City/State/Country

Tijuana Baja California, MX

Establishment Address

Guerrero Negro 2, Nordika Tijuana, Tijuana Baja California C.P. 22644, MX

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Precision Dynamics Corporation (Owner Number: 10042118)

Owner / Operator Contact Address

2221 W Camden Rd, Milwaukee, WI 53209, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SPEE-D-COOL COLD PACK SPEE-D-COOL COLD PACK, TROPICAL DESIGN SPEE-D-COOL COLD PACK, HEART SHAPED Process Indicator Steam Sterilization Tape Bandage Spee-D-Grid

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2014-04-25
JOJ	Indicator, Physical/Chemical Sterilization Process	General Hospital	Class 2	880.2800	2021-01-11
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2012-10-22
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2014-04-25

Official Correspondent

Ami Kern

US Agent Details

Ami Kern Business: Precision Dynamics Corporation Email: ami_kern@bradycorp.com Phone: (951) 6627265

Related Public Records

Same Entity

Precision Dynamics Corporation

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3011859755	Brady (Xiamen) Co. Ltd.	Xiamen Fujian, CN
3006079533	W. H. Brady S. de R.L. de C.V.	Tijuana Baja California, MX
3003450039	Brady Worldwide	Milwaukee, WI, US
2020282	PRECISION DYNAMICS CORPORATION	Valencia, CA, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
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

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2007	N/A	2	3M Comply 1248 Gas Plasma Chemical Indicator Strips for use in STERRAD 100, STERRAD 100S and STERRAD 50 Sterilization Systems. Indicator for hydrogen peroxide sterilant.

Similar Registrations

Registration Number	Establishment Name	Location
3037007193	SHANGHAI HUIZHOU INDUSTRIAL CO., LTD	Shanghai City District, CN
3031182683	NINGBO YAMAI INDUSTRY AND TRADE CO., LTD.	Yuyao Zhejiang, CN
3016711531	BRANCH IN PHU THO, THYGESEN TEXTILE VIETNAM COMPANY LIMITED	Yen Lap Commune Phu Tho, VN
3008384548	ACTIVE-ICE, INC.	Norman, OK, US
3002393819	MEDICAL SPECIALTIES OF CALIFORNIA LIMITED	Orpington Kent, GB

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010790521. Last updated year: 2026. Please use registration number 3010790521 when referencing this establishment in official correspondence.