FDA applicant
Beam-Med, Ltd.
FDA records 2 decisions for Beam-Med, Ltd. (Petach Tikva, IL) from 2000 to 2011: 1 510(k) clearance and 1 original PMA approval. All are in product code MUA (Bone Sonometer). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Beam-Med, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2011
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Beam-Med, Ltd.’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) ReportOther applicant names beginning “Beam-Med”
FDA records each applicant name separately; these may or may not be the same firm.