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Gesco Intl., Inc.

United StatesFDA applicant, unverified

Devices
26

What Gesco Intl., Inc. makes

Gesco Intl., Inc. manufactures various medical devices including catheters such as THORA-CATH, PER-Q-CATH, and UMBILI-CATH-S, as well as related products like repair kits, catheterization trays, and needles. They also produce obstetrical vacuum cups, spinal tap needles, and aspirators.

The company's portfolio includes Class I and Class II medical devices that are listed in the FDA 510(k) registry. Gesco Intl., Inc. is based in the US.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue26

Newest first, rows 1-26 of 26

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  • Thora-Cath Ref K941232

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

  • Per-Q-Cath Tray Ref K831845

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

  • Gesco Per-Q-Cath Repair Kit Ref K910622

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

  • Umbili-Cath-S Ref K940953

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

  • Gesco Catheterization Tray Ref K882647

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

  • Gesco Dual Lumen Umbilicath Ii-Dl Ref K896041

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

  • Gesco Per-Q-Cath Needle Ref K911215

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

  • Obstetrical Vacuum Cup Ref K911326

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

  • Per-Q-Cath Mid-Line Ref K954422

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

  • Umbili-Cath-S-Dl Ref K940952

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

  • Spinal Tap Needle Ref K910652

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

  • Gesco Aspirator Ref K870962

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

  • Dialy-Nate Set & Dialy-Nate Catheter Ref K872221

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

  • Gesco Per-Q-Cath Catheter Introducer Ref K915167

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

  • Thora-Cath Trocar-Type Chest Drainage Tube Ref K851385

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

  • Gesco Dual Lumen Per-Q-Cath-Dl Ref K895942

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

  • Uri-Cath Catheter Ref K941672

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

  • Umbili-Cath-P Ref K940871

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

  • Ventri-Cath Ref K931989

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

  • Umbili-Cath Ref K940870

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

  • Nutri-Cath - Feeding Tube Ref K861090

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

  • Catheter, Cholangiogram, Operative Ref K772288

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

  • Pala-Nate Ref K923591

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

  • Uri-Cath System Ref K852490

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

  • Gesco Umbili-Cath Ref K911607

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

  • Per-Q-Cath Dressing Change Tray Ref K926063

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

Rows 1-26 of 26

Frequently asked questions

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

The registry currently lists 26 devices for Gesco Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Gesco Intl., Inc.'s devices?

Among its 26 most recently registered devices, Gesco Intl., Inc. has devices listed in FDA 510(k) (26 devices).

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

Among its 26 most recently registered devices, the classes recorded for Gesco Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Gesco Intl., Inc. include THORA-CATH, PER-Q-CATH TRAY, GESCO PER-Q-CATH REPAIR KIT and UMBILI-CATH-S.

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