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Polamedco, Inc.

United StatesFDA applicant, unverified

Devices
20

What Polamedco, Inc. makes

Polamedco, Inc. manufactures airway management devices, including nasopharyngeal and nasotracheal airways, endotracheal tubes, and stylette guides for intubation. The company also produces surgical tools like cricothyrotomy tubes, an introscope for visual airway assessment, and a surgical eye protector. Additional products include gastric catheters for irrigation and aspiration, circuit connectors for ventilatory support, and cuffed endotracheal tube sets.

The company’s portfolio includes Class I and Class II medical devices, with several products listed under the FDA’s 510(k) clearance pathway. These devices are regulated under U.S. federal regulations and are intended for use in emergency airway management, surgical procedures, and respiratory support. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue20

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  • Flextitip Stylette Ref K950380

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

  • Linder Nasopharyngeal Airway Ref K843524

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

  • Linder Nasotracheal Airway Ref K881496

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

  • Airguide Stylette Ref K950713

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

  • Cricothyrotomy Tube Ref K983000

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

  • Sureloc Circuit Connector Ref K954383

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

  • Gastric, Catheter, Irrigation & Aspiration Ref K933596

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

  • Slick Endotracheal Tube Ref K812943

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

  • Visoshield(Tm), Surgical Eye Protector Ref K894516

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

  • Introscope Ref K953793

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

  • Polamedco Nasopaharyngeal Airway Ref K900456

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

  • Slick Set, Cuffed Ref K781808

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

  • Cuffed Linder Nasotracheal Airway Ref K900457

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

  • Sureloc External Connector Ref K791532

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

  • Slick Set Ref K780900 Open recall

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

  • Omnisurg Side Mounting Clamp & Rail Ext. Ref K821933

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

  • Omnisurg Working Instrument Table Ref K810150

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

  • Polamedco Tracheal And Nasotracheal Tubes Ref K920900

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

  • Gynesurg Ref K780587

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

  • Slick Set W/Sureloc External Connector Ref K810151

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

Rows 1-20 of 20

Frequently asked questions

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

The registry currently lists 20 devices for Polamedco, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Polamedco, Inc.'s devices?

Among its 20 most recently registered devices, Polamedco, Inc. has devices listed in FDA 510(k) (20 devices).

What risk classes do Polamedco, Inc.'s devices fall under?

Among its 20 most recently registered devices, the classes recorded for Polamedco, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Polamedco, Inc. include FLEXTITIP STYLETTE, LINDER NASOPHARYNGEAL AIRWAY, LINDER NASOTRACHEAL AIRWAY and AIRGUIDE STYLETTE.

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