FDA applicant
Devon Medical Products
FDA records 6 decisions for Devon Medical Products (King Of Prussia, PA) from 2012 to 2016: 6 510(k) clearances. Most are in product codes OMP (Negative Pressure Wound Therapy Powered…) and JOW (Sleeve, Limb, Compressible). Its devices cite 5 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Devon Medical Products, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Devon Medical Products’s devices, and how often a recall has named them.
FDA decisions per year
1in 2016
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2012.
Planning a device like Devon Medical Products’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 “Devon”
FDA records each applicant name separately; these may or may not be the same firm.