FDA applicant
Bmw Medical, Inc.
FDA records 5 decisions for Bmw Medical, Inc. (Salt Lake City, UT) from 1996 to 1997: 5 510(k) clearances. Most are in product codes LJS (Catheter, Intravascular, Therapeutic…) and FPA (Set, Administration, Intravascular). 11 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Bmw Medical, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Bmw Medical, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Bmw Medical, Inc.’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