FDA applicant
Medic One
FDA records 1 decision for Medic One (Independence, MO) in 1988: 1 510(k) clearance. All are in product code KGB (Mask, Oxygen, Non-Rebreathing). 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 Medic One’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medic One since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medic One’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 “Medic”
FDA records each applicant name separately; these may or may not be the same firm.