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Bemis Health Care

Country not established

Devices
12
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue12

Newest first, rows 1-12 of 12

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  • Carafe, Personal, 1-Qt Semi-Rectangular Ref K760072

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Critical Measurement Unit Ref K822556

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Suction Canister Ref K771737

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Bemis Sterile-Case For Use W/Ethylene Oxide Steri. Ref K885019

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Tumbler, Personal, Round, 9 Ounce Ref K760070

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Specimen Adaptor Ref K822557

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Suction Probe Ref K803206

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Bed Pan, Stackable (Autoclavable) Ref K760393

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • 8 Emesis Basin Ref K771733

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Male Urinal Ref K771738

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Tray, Personal, Rectang. 8 1/2 X 5 1/4 Ref K760071

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Basin, Wash, 6-Qt Rectangular Ref K760073

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

Rows 1-12 of 12

FDA recalls1

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

  • 2006

    • 23 Aug 2006 Z-0170-2007 Unclassified (pre-2012) Terminated The 5 Quart Wall Safes are shipped as two pieces (bottom & top) that customers are unable to assemble because of excess warp in the back wall of the container. Distribution: Nationwide and Canada. Submission numbers: K931664, K941664

Frequently asked questions

How many devices does Bemis Health Care have in the registry?

The registry currently lists 12 devices for Bemis Health Care. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bemis Health Care's devices?

Among its 12 most recently registered devices, Bemis Health Care has devices listed in FDA 510(k) (12 devices).

What risk classes do Bemis Health Care's devices fall under?

Among its 12 most recently registered devices, the classes recorded for Bemis Health Care's devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Bemis Health Care?

FDA recall records list 1 recall initiated by Bemis Health Care, the most recent initiated on 23 Aug 2006. 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 Bemis Health Care in the registry?

The most recently registered devices listed for Bemis Health Care include CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR, CRITICAL MEASUREMENT UNIT, SUCTION CANISTER and BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI..

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