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Catheter Technology Corp.

United StatesFDA applicant, unverified

Devices
13

What Catheter Technology Corp. makes

Catheter Technology Corp. makes vascular and umbilical catheters, including peripherally inserted central venous catheters, long-term Groshong catheters, umbilical vessel catheters, and cholangiography catheters. They also produce catheter repair kits and implantable vascular access systems such as port systems, along with diagnostic test kits labeled TESTCORP PREG, CRP, ANA, and ASO.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Catheter Technology Corp. is based in the United States.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

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  • Groshong Cv Catheter Repair Kit Ref K871998 Open recall

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

  • Testcorp Preg Ref K831366

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

  • Brawn And Groshong Catheters Ref K860256

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

  • Cath-Tech Polyurethane Umbilical Vess Ref K842577

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

  • Umbilical Vessel Catheter Ref K840339

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

  • Peripherally Inserted Central Venous Catheter Ref K871080

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

  • Cath-Tech Cholangiography Catheter Ref K842147

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

  • Groshong Catheter, Long Term Type Ref K831386

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

  • Cath-Tech Port Implantable Vascular Access System Ref K880571

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

  • Testcorp Crp Ref K831362

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

  • Testcorp Ana Ref K831365

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

  • Testcorp Aso Ref K831363

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

  • Beta-Preg Ref K831361

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Catheter Technology Corp. have in the registry?

The registry currently lists 13 devices for Catheter Technology Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Catheter Technology Corp.'s devices?

Among its 13 most recently registered devices, Catheter Technology Corp. has devices listed in FDA 510(k) (13 devices).

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

Among its 13 most recently registered devices, the classes recorded for Catheter Technology Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Catheter Technology Corp. in the registry?

The most recently registered devices listed for Catheter Technology Corp. include GROSHONG CV CATHETER REPAIR KIT, TESTCORP PREG, BRAWN AND GROSHONG CATHETERS and CATH-TECH POLYURETHANE UMBILICAL VESS.

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