FDA applicant
Medtrade Products, Ltd.
FDA records 23 decisions for Medtrade Products, Ltd. (Crewe, GB) from 2000 to 2023: 23 510(k) clearances. Most are in product codes QSY (Hemostatic Wound Dressing Without Thrombin Or…) and FRO (Dressing, Wound, Drug). Its devices cite 32 predicates, 15 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Medtrade Products Limited”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Medtrade Products, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2023
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medtrade 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) ReportOther applicant names beginning “Medtrade”
FDA records each applicant name separately; these may or may not be the same firm.