FDA applicant
Brimfield Scientific Instruments
FDA records 5 decisions for Brimfield Scientific Instruments (Walker, MI) from 1983 to 1985: 5 510(k) clearances. Most are in product codes GDG (Hook, Surgical, General & Plastic Surgery) and GDZ (Handle, Scalpel). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Brimfield Scientific Instruments’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Brimfield Scientific Instruments since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Brimfield Scientific Instruments’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report