Brady Worldwide

FDA Device Registration & Listing · Milwaukee, WI, US · Registration 3003450039

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
3003450039
FEI Number
3003450039
Entity Name
Brady Worldwide
City/State/Country
Milwaukee, WI, US
Establishment Address
2221 W Camden Rd, Milwaukee, WI 53209, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Precision Dynamics Corporation (Owner Number: 2020282)
Owner / Operator Contact Address
2221 W Camden Rd, Milwaukee, WI 53209, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Armboard, Wristboard Spee-D-Grid Spee-D-Grid SGRID1 SGRID2 SGRID3 SGRID-X1 Sterile Medication Labels Left Marker, Right Marker Spee-D-Stretch Repositionable, Spee-D-Line, Spee-D-Mark CT and MRI Super-Sticky Spee-D-Strip, Spee-D-Line Radiology Skin Marker, Mammography Skin Marker Spee-D-Mark, Spee-D-Arrow, Spee-D-Angle, Spee-D-Strip, Spee-D-Stretch CT Scan Skin Markers, MRI Skin Markers No Burnout, Scar Marker, Nipple Marker, Mole Marker, Ring Marker Spee-D brand X-Ray Skin Markers

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IZH System, X-Ray, Mammographic Radiology Class 2 892.1710 2016-07-19
NOD Board, Arm (With Cover), Non-Sterile General, Plastic Surgery Class 1 878.3910 2021-10-11
NNI Container, Specimen, Non-Sterile Pathology Class 1 864.3250 2014-04-30
LYV Label Or Tag, Sterile General, Plastic Surgery Class 1 878.4800 2013-11-20
HFM Monitor, Uterine Contraction, External (For Use In Clinic) Obstetrics/Gynecology Class 2 884.2720 2011-12-05
JAC System, X-Ray, Film Marking, Radiographic Radiology Class 1 892.1640 2013-11-20

Official Correspondent

Ami Kern

US Agent Details

No US Agent registered (Local establishment).

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
2020282 PRECISION DYNAMICS CORPORATION Valencia, CA, US
3010790521 Brady Mexico, S. de R.L. de C.V. Tijuana Baja California, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K040392 American I.V. Products, Inc. TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORING 2004-09-14
K992811 Epic Medical Equipment Services, Inc. TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORING 2000-01-18

Similar Registrations

Registration Number Establishment Name Location
2618282 BD Puerto Rico LLC Juncos, PR, US
1056553 REMINGTON MEDICAL, INC. ALPHARETTA, GA, US
3007014520 Remington Medical, Inc. Alpharetta, GA, US
3010703925 MAKAR CONSULTING PTY LTD Belrose New South Wales, AU
3043048939 CANADIAN IMAGING SERVICES INC. Edmonton Alberta, CA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003450039. Last updated year: 2026. Please use registration number 3003450039 when referencing this establishment in official correspondence.
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