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Sentry Medical Products, Inc.

United StatesFDA applicant, unverified

Devices
13

What Sentry Medical Products, Inc. makes

Sentry Medical Products, Inc. manufactures single-use and reusable medical electrodes, adhesive belts, and disposable dispersive pads for electrocardiogram (ECG) monitoring, transcutaneous electrical nerve stimulation (TENS), and temperature measurement. Their product line includes radiolucent ECG electrodes for imaging compatibility, infant-specific electrode belts, and reusable insertion trays for electrode application. Additional offerings include patient cables, leadwires, and temperature monitoring devices like the AccuTemp Plus.

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Products are listed in the FDA’s 510(k) database, reflecting their regulatory status in the United States. The manufacturer operates from its base in the US.

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

Catalogue13

Newest first, rows 1-13 of 13

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  • Sentry Radiotranslucent Ecg Electrodes Ref K962122

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

  • Duraderm Butterfly Ref K881343

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

  • Sentry Flexible Tens Ref K853552

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

  • Sentry Insertion Tray Ref K942827

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

  • Diagnostic Ecg Disposable Electrode Ref K851522

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

  • Infant Electrode Belt Ref K830362

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

  • Baby Board Ref K935098

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

  • Sentry Disposable Dispersive Electrode Ref K955636

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

  • Accutemp Plus Ref K881670

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

  • Patient Cable Ref K932704

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

  • Sentry Aqueous Gel Ecg Electrodes Ref K934000

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

  • Leadwire Ref K933603

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

  • Infant Limb Electrode Ref K844632

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Sentry Medical Products, Inc. have in the registry?

The registry currently lists 13 devices for Sentry Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sentry Medical Products, Inc.'s devices?

Among its 13 most recently registered devices, Sentry Medical Products, Inc. has devices listed in FDA 510(k) (13 devices).

What risk classes do Sentry Medical Products, Inc.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Sentry Medical Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Sentry Medical Products, Inc. in the registry?

The most recently registered devices listed for Sentry Medical Products, Inc. include SENTRY RADIOTRANSLUCENT ECG ELECTRODES, DURADERM BUTTERFLY, SENTRY FLEXIBLE TENS and SENTRY INSERTION TRAY.

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