FDA applicant
Mars Medical Products
FDA records 4 decisions for Mars Medical Products (Crofton, MD) from 1998 to 2005: 4 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). No recall is linked to its devices.
FDA’s records also spell it “Mars Medical Products Co., Ltd.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Mars Medical Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Mars Medical Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Mars 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 “Mars”
FDA records each applicant name separately; these may or may not be the same firm.