FDA applicant

Rifton Equipment For the Handicapped

Rifton, NY7 decisions1989–19920 recalls

FDA records 7 decisions for Rifton Equipment For the Handicapped (Rifton, NY) from 1989 to 1992: 7 510(k) clearances. Most are in product codes INW (Table, Mechanical) and INN (Chair, Adjustable, 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 Rifton Equipment For the Handicapped’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rifton Equipment For the Handicapped since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rifton Equipment For the Handicapped by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Other applicant names beginning “Rifton”

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

Rifton 1

Rifton Equipment For the Handicapped

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rifton”