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Venospital, Inc.

United StatesFDA applicant, unverified

Devices
14

What Venospital, Inc. makes

Venospital, Inc. manufactures infusion sets and hemodialysis fistula sets, including models like the Venothin series (sizes 19, 21, 23, and 25) and specialized infusion sets with injection sites. The company also produces venous access devices such as the Flu-Ven series (e.g., Flu-Ven 0150, 01510, and TR-1), designed for fluid administration and hemodialysis applications.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. Venospital, Inc. is based in the United States.

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

Catalogue14

Newest first, rows 1-14 of 14

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  • Infusion Set, Venothin 21 Ref K781190

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

  • Flu-Ven 01510 Ref K790424

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

  • Infusion Set, Venothin 25 Ref K781188

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

  • Flu Ven 0160 Ref K770863

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

  • Infusion Set W/ Injection Site Ref K781185

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

  • Hemodialysis Fistula Set Ref K770864

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

  • Flu Ven Tr-1 Ref K791131

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

  • Flu Ven 0150 Ref K771362

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

  • Infusion, Venothin 23 Ref K781186

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

  • Flu Ven 0151 Ref K781189

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

  • Infusion Set, Venothin 19 Ref K781184

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

  • Flu-Ven Tk-2 Ref K791130

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

  • Biostil # 3884 Ref K790077

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

  • Infusion Set W/ Injection Site, 23D-W Ref K781187

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

Rows 1-14 of 14

Frequently asked questions

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

The registry currently lists 14 devices for Venospital, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Venospital, Inc.'s devices?

Among its 14 most recently registered devices, Venospital, Inc. has devices listed in FDA 510(k) (14 devices).

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

Among its 14 most recently registered devices, the classes recorded for Venospital, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Venospital, Inc. include INFUSION SET, VENOTHIN 21, FLU-VEN 01510, INFUSION SET, VENOTHIN 25 and FLU VEN 0160.

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