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Lumiscope Co., Inc.

United StatesFDA applicant, unverified

Devices
13

What Lumiscope Co., Inc. makes

Lumiscope Co., Inc. manufactures a range of medical devices including blood pressure monitors, infrared lamps, and thermometers. Their portfolio also features therapeutic equipment such as TENS units, interferential current therapy units, EMS devices, and alternating pressure pads with pumps, alongside various electrodes and cardiac monitoring equipment.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

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  • Lumiscope Model 1000/Apcc Model 1000 Ref K894127

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

  • Lumisonic Ref K924081

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

  • Infrared Lamp Ref K925054

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

  • Cardicare Model Mt-301F & Mt-301C Ref K032714

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

  • Lumiscope Electrodes Models El-08, 11, 15, 06, 21, 25 Ref K901809

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

  • Lumiscope Ems 8000 Ref K901849

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

  • Interferential Current Therapy Unit Ref K931768

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

  • Lumiscope Tens Model 2000T Or Apcc 3001 Or Pain Re Ref K880452

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

  • Lumiscope Micro 100 Ref K901726

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

  • Gymman Ref K920099

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

  • Lumiscope Model 2018 Thermometer Ref K954792

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

  • Lumiscope Alternating Pressure Pad & Pump Ref K901096

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

  • Lumineb I Ref K884722

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

Rows 1-13 of 13

Frequently asked questions

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

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

Which registries list Lumiscope Co., Inc.'s devices?

Among its 13 most recently registered devices, Lumiscope Co., Inc. has devices listed in FDA 510(k) (13 devices).

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

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

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

The most recently registered devices listed for Lumiscope Co., Inc. include LUMISCOPE MODEL 1000/APCC MODEL 1000, LUMISONIC, INFRARED LAMP and CARDICARE MODEL MT-301F & MT-301C.

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