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Kingswood Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
3
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Kingswood Laboratories, Inc. makes

Kingswood Laboratories, Inc. manufactures single-use oral swabs and throat swab devices designed for collecting and transporting clinical samples, including the MOI-STIR Oral Swabstick and the THROAT MOI-STIR.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Throat Moi-Stir Ref K840807

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Moi-Stir Oral Swabstick(S) Ref K851026

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Moi-Stir Ref K810157

    Active Regimes: 510(k) Registry: 510(k) Class:—

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 1 recall initiated by Kingswood Laboratories, Inc., initiated on 2005-04-22. By recorded status: 1 terminated. The reasons filed fall into these groups: sterility or contamination. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2005

    • 22 Apr 2005 Z-0820-05 Unclassified (pre-2012) Terminated Contaminated with Aspergillus and Penicillum molds. Distribution: Nationwide. Submission number: K851026

Frequently asked questions

How many devices does Kingswood Laboratories, Inc. have in the registry?

The registry currently lists 3 devices for Kingswood Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kingswood Laboratories, Inc.'s devices?

Among its 3 most recently registered devices, Kingswood Laboratories, Inc. has devices listed in FDA 510(k) (3 devices).

Are there FDA recall records for Kingswood Laboratories, Inc.?

FDA recall records list 1 recall initiated by Kingswood Laboratories, Inc., the most recent initiated on 22 Apr 2005. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Kingswood Laboratories, Inc. in the registry?

The most recently registered devices listed for Kingswood Laboratories, Inc. include THROAT MOI-STIR, MOI-STIR ORAL SWABSTICK(S) and MOI-STIR.

Generated automatically from registry data and not verified by a human reviewer.