510(k) Report

FDA applicant

Vail Products, Inc.

Toledo, OH4 decisions1996–19982 recalls

FDA records 4 decisions for Vail Products, Inc. (Toledo, OH) from 1996 to 1998: 4 510(k) clearances. Most are in product codes FNL (Bed, Ac-Powered Adjustable Hospital) and FMS (Bed, Pediatric Open Hospital). 2 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, general hospital panel, where it files most

How often FDA has decided Vail Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vail Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vail Products, 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?

  • FNLBed, Ac-Powered Adjustable Hospital3decisions
  • FMSBed, Pediatric Open Hospital1decision

What has FDA decided for it lately?

  • K982783Vail 1000 Enclosed BedVail Products, Inc. · 19981 recall
  • K963622Vail 2000 Enclosed BedVail Products, Inc. · 19971 recall
  • K963589Vail 3000 Bed EnclosureVail Products, Inc. · 1997
  • K963210Vail 100 Pediatric CribVail Products, Inc. · 1996

All 4 as Vail Products, Inc. →

What has been recalled?

2 recalls linked to its devices; the latest:

  • K982783Vail 1000 Enclosed Bed System.May 6, 2005
  • K963622Vail 2000 Enclosed Bed System.May 6, 2005