510(k) Report

FDA applicant

Reliance Medical Corp.

Grand Junction, CO3 decisions1985–20010 recalls

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, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

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.

FIG. 1 — Reliance Medical Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Reliance”

FDA records each applicant name separately; these may or may not be the same firm.