FDA applicant

Macbrud Corp. Medical Div.

Miami, FL4 decisions1989–19910 recalls

FDA records 4 decisions for Macbrud Corp. Medical Div. (Miami, FL) from 1989 to 1991: 4 510(k) clearances. Most are in product codes KDD (Kit, Surgical Instrument, Disposable) and JAC (System, X-Ray, Film Marking, Radiographic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

How often FDA has decided Macbrud Corp. Medical Div.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Macbrud Corp. Medical Div. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Macbrud Corp. Medical Div. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Macbrud”

FDA records each applicant name separately; these may or may not be the same firm.

Macbrud Corp., Medical Division 1

Macbrud Corp. Medical Div.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Macbrud”