FDA applicant
Beecher Medical Diagnostic Instrumentation
FDA records 3 decisions for Beecher Medical Diagnostic Instrumentation (Silver Spring, MD) from 1984 to 1987: 3 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and GDI (Dissector, Surgical, General & Plastic Surgery). 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 Beecher Medical Diagnostic Instrumentation’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Beecher Medical Diagnostic Instrumentation since 2007.
Recalls per year
No recall linked to its devices since 2007.
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