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Futuremed Div. of Future Impex Corp.

United StatesFDA applicant, unverified

Devices
17

What Futuremed Div. of Future Impex Corp. makes

Futuremed manufactures diagnostic and therapeutic medical devices, including spirometers (such as the ST-460, ST-90, and ST-250/ST-300 models) for pulmonary function testing, audiometers (e.g., the DA 323) for hearing assessment, and transcutaneous electrical nerve stimulation (TENS) devices for chronic pain relief. Their portfolio also includes carbon electrodes, conductivity gels for electrode adhesion, and latex surgical gloves. A selector device (SL 01) is listed among their offerings.

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 U.S. Food and Drug Administration’s 510(k) clearance registry. Futuremed is based in the United States.

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

Catalogue17

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  • Spirovision Ref K864885

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

  • Carbon Electrode Ref K872044

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

  • Selector Sl 01 Ref K933220

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

  • Conductivity Gel Ref K871913

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

  • Conductivity Gel Ref K872045

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

  • Tens Device For Relief Of Chronic Pain Ref K864114

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

  • St-460 Spiro Analyzer Spirometer Ref K852308

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

  • Audiometer Da 323 Ref K933222

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

  • Upgraded Spirometer St-90 Ref K933511

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

  • Latex Surgical Gloves Ref K864064

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

  • Spiro Analyzer Model St 250 Ref K901308

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

  • Spiro Analyzer St-300 Ref K873817

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

  • Model Hl-100 Portable Dc Elect. Therapeutic Unit Ref K871421

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

  • Pulmonary Test System Fudac-30 Ref K852307

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

  • Mega-Tens Dual Channel T.E.N.S. Ref K903017

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

  • Futuremed Ecg System 500 Ref K862381

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

  • Transcoutaneous Electro-Neuro Stimulator Ref K884972

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

Rows 1-17 of 17

Frequently asked questions

How many devices does Futuremed Div. of Future Impex Corp. have in the registry?

The registry currently lists 17 devices for Futuremed Div. of Future Impex Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Futuremed Div. of Future Impex Corp.'s devices?

Among its 17 most recently registered devices, Futuremed Div. of Future Impex Corp. has devices listed in FDA 510(k) (17 devices).

What risk classes do Futuremed Div. of Future Impex Corp.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for Futuremed Div. of Future Impex Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Futuremed Div. of Future Impex Corp. in the registry?

The most recently registered devices listed for Futuremed Div. of Future Impex Corp. include SPIROVISION, CARBON ELECTRODE, SELECTOR SL 01 and CONDUCTIVITY GEL.

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