FDA applicant
Biomedics
FDA records 10 decisions for Biomedics (Los Angeles, CA) from 1980 to 1999: 10 510(k) clearances. Most are in product codes JEY (Plate, Bone) and JDI (Prosthesis, Hip, Semi-Constrained…). 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 Biomedics’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Biomedics since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Biomedics’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