510(k) Report

FDA applicant

Eagle Parts & Products, Inc.

Augusta, GA2 decisions1999–19992 recalls

FDA records 2 decisions for Eagle Parts & Products, Inc. (Augusta, GA) in 1999: 2 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Eagle Parts & Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eagle Parts & Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Eagle”

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