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Cottrell, Ltd.

Country not established

Devices
9

What Cottrell, Ltd. makes

Cottrell, Ltd. manufactures a range of medical device products for infection control and sterilization, including barrier films, sterilization pouches, and chemical sterilants. Their portfolio includes self-sealing sterilization pouches, liquid sterilants with activators, and concentration indicators for disinfectants. The company also produces overgloves and barrier tubes designed for medical procedures, as well as sporicidal solutions for high-level disinfection.

The company’s products are regulated under the FDA’s 510(k) pathway, with devices classified as either Class I or Class II. These products are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

  • Pro Barrier(Tm) Tube Sox(Tm) Ref K945575

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Vapocide Ref K970726

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Proview Self-Sealing Sterilization Pouch Ref K893802

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Procide 14 N.S., Omnicide/Liquid & Plus Liq Activator Ref K932922

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Protouch Overglove Ref K952241

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Barrier All Film Ref K952234

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Imni-Ii Ref K951983

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Prochek G Glutaraldehyde Concentration Level Indicator Ref K960089

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Endo-Spor Plus / Hyprocide Ref K972708

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

Frequently asked questions

How many devices does Cottrell, Ltd. have in the registry?

The registry currently lists 9 devices for Cottrell, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cottrell, Ltd.'s devices?

Among its 9 most recently registered devices, Cottrell, Ltd. has devices listed in FDA 510(k) (9 devices).

What risk classes do Cottrell, Ltd.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Cottrell, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cottrell, Ltd. in the registry?

The most recently registered devices listed for Cottrell, Ltd. include PRO BARRIER(TM) TUBE SOX(TM), VAPOCIDE, PROVIEW SELF-SEALING STERILIZATION POUCH and PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR.

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