FDA applicant
Dumex Medical Surgical Products, Ltd.
FDA records 13 decisions for Dumex Medical Surgical Products, Ltd. (Toronto, Orntario, CA) from 1994 to 2000: 13 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and EFQ (Gauze/Sponge, Internal). 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 Dumex Medical Surgical Products, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Dumex Medical Surgical Products, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Dumex Medical Surgical Products, 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