510(k) Report

FDA applicant

Ryan Medical, Inc.

Brentwood, TN5 decisions1988–19920 recalls

FDA records 5 decisions for Ryan Medical, Inc. (Brentwood, TN) from 1988 to 1992: 5 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FMI (Needle, Hypodermic, Single Lumen). 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 Ryan Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ryan Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ryan Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Ryan”

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