FDA applicant
Dilon Medical Technologies, Ltd.
FDA records 1 decision for Dilon Medical Technologies, Ltd. (Business Park-South 3088900) in 2012: 1 original PMA approval. All are in product code OEE (Diagnostic Low Electric Field). 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 Dilon Medical Technologies, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2012
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2012.
Planning a device like Dilon Medical Technologies, 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 “Dilon”
FDA records each applicant name separately; these may or may not be the same firm.