510(k) Report

FDA applicant

Ted Hoyer & Co., Inc.

Oshkosh, WI2 decisions1986–19860 recalls

FDA records 2 decisions for Ted Hoyer & Co., Inc. (Oshkosh, WI) in 1986: 2 510(k) clearances. Most are in product codes FSA (Lift, Patient, Non-Ac-Powered) and FRW (Scale, Patient). 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, general hospital panel, where it files most

How often FDA has decided Ted Hoyer & Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ted Hoyer & Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ted Hoyer & Co., 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?

  • FSALift, Patient, Non-Ac-Powered1decision
  • FRWScale, Patient1decision

What has FDA decided for it lately?

  • K862477Hoyer Digital Electronic ScaleTed Hoyer & Co., Inc. · 1986
  • K860837Hoyer One-Touch Power LifterTed Hoyer & Co., Inc. · 1986

All 2 as Ted Hoyer & Co., Inc. →