FDA applicant
A.D.T. Lab Industries
FDA records 21 decisions for A.D.T. Lab Industries (Mchenry, IL) from 1980 to 1981: 21 510(k) clearances. Most are in product codes GAA (Needle, Aspiration And Injection, Disposable) and FCG (Biopsy Needle). 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 A.D.T. Lab Industries’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for A.D.T. Lab Industries since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like A.D.T. Lab Industries’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