FDA applicant
Reliance Medical Corp.
FDA records 3 decisions for Reliance Medical Corp. (Grand Junction, CO) from 1985 to 2001: 3 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and QPB (System, Suction, Lipoplasty For Removal). 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 Reliance Medical Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Reliance Medical Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Reliance Medical Corp.’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 “Reliance”
FDA records each applicant name separately; these may or may not be the same firm.