FDA applicant
B&B Medical Technologies, Inc.
FDA records 23 decisions for B&B Medical Technologies, Inc. (Rancho Cordova, CA) from 1986 to 2004: 23 510(k) clearances. Most are in product codes CBH (Device, Fixation, Tracheal Tube) and CAF (Nebulizer (Direct Patient Interface)). 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 B&B Medical Technologies, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for B&B Medical Technologies, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like B&B Medical Technologies, 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