FDA applicant
A&D Engineering, Inc.
FDA records 34 decisions for A&D Engineering, Inc. (Milpitas, CA) from 1987 to 2008: 34 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and DSK (Computer, Blood-Pressure). Its devices cite 15 predicates, 15 of them its own earlier devices. 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided A&D Engineering, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2008
2026 so far, outlined.
Recalls per year
1in 2016
Class I Class II/III not classified
Planning a device like A&D Engineering, 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