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Data / Medical devices / United States / Macbrud Corp., Medical Division

Macbrud Corp., Medical Division: FDA-registered device maker in Crossings, FL, United States, 2 510(k) clearances

Macbrud Corp., Medical Division is registered with the FDA (registration 1052243) in Crossings, FL, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated January 11, 2013. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
1052243
Address
12101 SW 131 Avenue, Crossings, FL, United States, 33186
Owner or operator
MACBRUD CORP., MEDICAL DIVISION (1052243)
Roles
Manufacturer
First device listed
January 16, 2013
Registered through
2026
Brand names listed
SPECBOARD JR

Devices it lists

DeviceProduct codeClassRoleSource
System, X-Ray, MammographicIZH2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 11, 2013K123414SPECBOARD JR.IZHSubstantially EquivalentMacbrud Corp., Medical Divisionaccessdata.fda.gov
April 7, 1989K891090SPECBOARDIZHSubstantially EquivalentMacbrud Corp. Medical Div.accessdata.fda.gov

Compare with other makers

Updated January 11, 2013. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.