510(k) Report

FDA applicant

Crow River Industries, Inc.

Plymouth, MN4 decisions1990–19953 recalls

FDA records 4 decisions for Crow River Industries, Inc. (Plymouth, MN) from 1990 to 1995: 4 510(k) clearances. All are in product code ING (Elevator, Wheelchair, Portable). 3 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 Crow River Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Crow River Industries, Inc. since 2007.

Recalls per year

3in 2007

2007: 3
2007high 3 (2007) · low 0 (2008)2026

Class I Class II/III not classified

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

Planning a device like Crow River Industries, Inc.’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

Which product codes does it file in?

  • INGElevator, Wheelchair, Portable4decisions

What has FDA decided for it lately?

  • K952946Vangator IICrow River Industries, Inc. · 19953 recalls
  • K922624Ultragater Wheelchair LiftCrow River Industries, Inc. · 1992
  • K901989Gravity Down Wheelchair LiftCrow River Industries, Inc. · 1990
  • K900417Wheelchair Lift (Wheelchair Elevator)Crow River Industries, Inc. · 1990

All 4 as Crow River Industries, Inc. →

What has been recalled?

3 recalls linked to its devices; the latest:

  • K952946Braun wheelchair lift, model NL, Braun Corporation, Winamac, IN A wheelchair lift for…Aug 15, 2007
  • K952946Braun wheelchair lift, model NCL, Braun Corporation, Winamac, IN A wheelchair lift for…Aug 15, 2007
  • K952946Braun wheelchair lift, model NVL, Braun Corporation, Winamac, IN A wheelchair lift for…Aug 15, 2007