FDA applicant

Advanced Biomedical Instruments

Walker, MI4 decisions1980–19840 recalls

FDA records 4 decisions for Advanced Biomedical Instruments (Walker, MI) from 1980 to 1984: 4 510(k) clearances. Most are in product codes HFB (Forceps, Biopsy, Gynecological) and HHR (Laser, Surgical, Gynecologic). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Advanced Biomedical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Biomedical Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Biomedical Instruments by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Advanced Biomedical Instruments

Which product codes does it file in?

What has FDA decided for it lately?