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Euro-Med Intl.

Country not established

Devices
16

What Euro-Med Intl. makes

Euro-Med Intl. manufactures surgical instruments for general and gynecological procedures, including cutting tools like knives and scissors, probing and grasping devices such as hook probes and graspers, and specialized curettes for tissue removal. Their portfolio also includes measurement tools like rulers and forceps for retrieval or stabilization, as well as instruments for controlled tissue incision, such as episiotomy scissors.

The company’s devices are classified under FDA categories Class I and Class II, with regulatory submissions recorded in the FDA’s 510(k) database. These instruments are intended for use in surgical settings and are subject to compliance with U.S. medical device regulations. The manufacturer operates from the United States.

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

Catalogue16

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  • Knife Ref K854891

    Class I
    Active 510(k) 510(k) I
  • Hook Scissor Ref K854896

    Class I
    Active 510(k) 510(k) I
  • Kevor-Curette Ref K882404

    Class II
    Active 510(k) 510(k) II
  • Ruler Ref K854892

    Class I
    Active 510(k) 510(k) I
  • Episiotomy Scissors Ref K854900

    Not classified
    Active 510(k) 510(k) —
  • Hook Probe Ref K854890

    Class I
    Active 510(k) 510(k) I
  • Randall Curette Ref K854888

    Class I
    Active 510(k) 510(k) I
  • Flex-I-Grasp Ref K854889

    Class II
    Active 510(k) 510(k) II
  • Novak Curette Ref K854899

    Class I
    Active 510(k) 510(k) I
  • Basket Forcep Ref K854895

    Class I
    Active 510(k) 510(k) I
  • Pacific Grasper Ref K854901

    Class I
    Active 510(k) 510(k) I
  • Spoon Ref K854894

    Class I
    Active 510(k) 510(k) I
  • Atlantic Grasper Ref K854898

    Class I
    Active 510(k) 510(k) I
  • Keyes Skin Punch Ref K854893

    Not classified
    Active 510(k) 510(k) —
  • Prostatic Core-Cut Needle Ref K883884

    Class II
    Active 510(k) 510(k) II
  • Max-I-Grasp Ref K854897

    Class I
    Active 510(k) 510(k) I

Rows 1-16 of 16

Frequently asked questions

How many devices does Euro-Med Intl. have in the registry?

The registry currently lists 16 devices for Euro-Med Intl.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Euro-Med Intl.'s devices?

Among its 16 most recently registered devices, Euro-Med Intl. has devices listed in FDA 510(k) (16 devices).

What risk classes do Euro-Med Intl.'s devices fall under?

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

What are the newest devices from Euro-Med Intl. in the registry?

The most recently registered devices listed for Euro-Med Intl. include KNIFE, HOOK SCISSOR, KEVOR-CURETTE and RULER.

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