# Dumex Medical Surgical Products, Ltd.

- Location (FDA's records): Toronto, Orntario, CA
- FDA decisions: 13 (1994–2000): 13 510(k) clearances
- Product codes: FRO (3), EFQ (3), KMF (2), MGQ (2), GDY (1), FOZ (1), NAD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K992732: Sterile Water & Sterile 0.9% Sodium Chloride (Apr 20, 2000)
- K993119: Sterile Hydrogel (Nov 23, 1999)
- K990332: Dumex Iodoform Packing Strip (Apr 14, 1999)
- K980779: Thalafix Natural Sea Salt Dressing (Jun 26, 1998)
- K980861: Dumex Pak-Its Cotton Gauze Packing Impregnated with Hydrogel (May 20, 1998)
- K980863: Dumex Pak-Its Non-Woven Dressing Impregnated Sith Sodium Chloride (Hypertonic) (May 11, 1998)
- K980777: Dumex Pak-Its-Absorbasalt Cotton Gauze Packing (May 4, 1998)
- K980791: Dumex Pak-Its Woven Ribbon Packing (Apr 29, 1998)

Source page: https://510kreport.com/company/dumex-medical-surgical-products