510(k) Report

FDA applicant

Kingswood Laboratories, Inc.

Mchenry, IL3 decisions1981–19851 recall

FDA records 3 decisions for Kingswood Laboratories, Inc. (Mchenry, IL) from 1981 to 1985: 3 510(k) clearances. All are in product code LFD (Saliva, Artificial). 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

No FDA decision for Kingswood Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kingswood Laboratories, 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?

  • LFDSaliva, Artificial3decisions

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K810157Moi-StirKingswood Laboratories, Inc. · 19811cites it
  • K840807Throat Moi-StirKingswood Laboratories, Inc. · 19841cites it

What has FDA decided for it lately?

  • K851026Moi-Stir Oral Swabstick (S)Kingswood Laboratories, Inc. · 19851 recall
  • K840807Throat Moi-StirKingswood Laboratories, Inc. · 1984
  • K810157Moi-StirKingswood Laboratories, Inc. · 1981

All 3 as Kingswood Laboratories, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K851026Moi-Stir oral swabsticks, an aid to mouth care and oral hygiene, CONTENTS: 3…Apr 22, 2005