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Clinipad Corp.

United StatesFDA applicant, unverified

Devices
16

What Clinipad Corp. makes

Clinipad Corp. manufactures single-use medical trays and kits for procedural and wound care, including tracheostomy care, catheter maintenance, and biopsy procedures. Their portfolio also covers sterile dressing and preparation kits, as well as accessories like spike guards and vascular access devices. These products are designed for use in operating rooms, clinical settings, and patient care environments.

The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. They are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue16

Newest first, rows 1-16 of 16

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  • Cliniguard Ref K800527

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

  • Tracheostomy Care Tray Ref K932016

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

  • Catheter Maintenance Kit Ref K811247

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

  • Wet Dressing Kit Ref K833075

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

  • Spike Guard Ref K812130

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

  • Punch Biopsy Kit Ref K862562

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

  • Picc Insertion Tray Ref K931668

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

  • V.A.D. Access Kit Ref K932010

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

  • Cliniguard Sterile Ref K810240

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

  • Subclavian Insertion Kit Ref K820171

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

  • Or Prep Kit Ref K830476

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

  • Cardiac Catheterization Tray Ref K931560

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

  • Laceration Tray Ref K932036

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

  • I.V. Start Kit Ref K932071

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

  • Catheter Insertion Kit Ref K833432

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

  • Tracheostomy Cleansing Solution Ref K862563

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

Rows 1-16 of 16

Frequently asked questions

How many devices does Clinipad Corp. have in the registry?

The registry currently lists 16 devices for Clinipad Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clinipad Corp.'s devices?

Among its 16 most recently registered devices, Clinipad Corp. has devices listed in FDA 510(k) (16 devices).

What risk classes do Clinipad Corp.'s devices fall under?

Among its 16 most recently registered devices, the classes recorded for Clinipad Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Clinipad Corp. in the registry?

The most recently registered devices listed for Clinipad Corp. include CLINIGUARD, TRACHEOSTOMY CARE TRAY, CATHETER MAINTENANCE KIT and WET DRESSING KIT.

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