FDA applicant
Andronic Devices, Ltd.
FDA records 16 decisions for Andronic Devices, Ltd. (Richmond,B.C. V6v-2j2, CA) from 1987 to 1994: 16 510(k) clearances. Most are in product codes JEA (Table, Surgical With Orthopedic Accessories…) and KKX (Drape, Surgical, Antimicrobial). 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 Andronic Devices, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Andronic Devices, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Andronic Devices, Ltd.’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