FDA applicant

Wheel Ring, Inc.

Manchester, CT1 decision1985–19850 recalls

FDA records 1 decision for Wheel Ring, Inc. (Manchester, CT) in 1985: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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 Wheel Ring, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wheel Ring, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wheel Ring, 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 “Wheel”

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

Wheel Checkers 2

Wheel Ring, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Wheel”