510(k) Report

FDA applicant

Snug Seat, Inc.

Stallings, NC2 decisions1994–19981 recall

FDA records 2 decisions for Snug Seat, Inc. (Stallings, NC) from 1994 to 1998: 2 510(k) clearances. All are in product code IOR (Wheelchair, Mechanical). 1 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 Snug Seat, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Snug Seat, Inc. since 2007.

Recalls per year

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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Which product codes does it file in?

  • IORWheelchair, Mechanical2decisions

What has FDA decided for it lately?

  • K982849Panther WheelchairSnug Seat, Inc. · 1998
  • K934560Wizard Pediatric WheelchairSnug Seat, Inc. · 19941 recall

All 2 as Snug Seat, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K934560Crocodile (size 3) are two-armed, wheeled walking aids, used by children with…Aug 26, 2013Class II