FDA applicant
Advanced Instrument Development, Inc.
FDA records 5 decisions for Advanced Instrument Development, Inc. (Melrose Park, IL) from 1979 to 1998: 5 510(k) clearances. Most are in product codes IZO (Generator, High-Voltage, X-Ray, Diagnostic) and KPR (System, X-Ray, Stationary). 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 Advanced Instrument Development, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Advanced Instrument Development, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Advanced Instrument Development, 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