510(k) Report

FDA applicant

Specialty Drives Technologies, Inc.

Winder, GA1 decision2002–20020 recalls

FDA records 1 decision for Specialty Drives Technologies, Inc. (Winder, GA) in 2002: 1 510(k) clearance. All are in product code ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Specialty Drives Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Specialty Drives Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Specialty Drives Technologies, 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 “Specialty”

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