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Amkor Trading Co.

Country not established

Devices
6

What Amkor Trading Co. makes

Amkor Trading Co. manufactures medical devices including scalp vein sets, hypodermic needles, solution infusion sets, blood transfusion sets, blood donor sets, and disposable syringes under the Hesung brand.

These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

  • Hesung Scalp Vein Set Ref K841564

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Hesung's Hyperdermic Needles Ref K841565

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Hesung's Solution Infusion Sets Ref K841563

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Hesung Blood Transfusion Sets Ref K841562

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Hesung's Blood Donor Sets Ref K841561

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Hesung Disposable Syringe Ref K841566

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

Frequently asked questions

How many devices does Amkor Trading Co. have in the registry?

The registry currently lists 6 devices for Amkor Trading Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Amkor Trading Co.'s devices?

Among its 6 most recently registered devices, Amkor Trading Co. has devices listed in FDA 510(k) (6 devices).

What risk classes do Amkor Trading Co.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Amkor Trading Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Amkor Trading Co. in the registry?

The most recently registered devices listed for Amkor Trading Co. include HESUNG SCALP VEIN SET, HESUNG'S HYPERDERMIC NEEDLES, HESUNG'S SOLUTION INFUSION SETS and HESUNG BLOOD TRANSFUSION SETS.

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