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C. Intl.

Country not established

Devices
7

What C. Intl. makes

C. Intl. manufactures obstetric and gynecological examination tools, including vaginal specula (VAGI-PRESS, VAGI-SPEC), forceps for catheterization and delivery (FORCEPS #101, #102, CATHETERIZATION FORCEP), and a proctoscope (PROCTOSCOPE #501). The portfolio also includes diagnostic aids like the EASY-SPEC and surgical accessories such as the SURGICAL DRAPE CLIP #201.

The company’s devices are classified under FDA’s Class I and Class II categories, with relevant products listed via the 510(k) pathway. These products are intended for use in the United States, where the manufacturer is based.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

  • Vagi-Press #401 Ref K790851

    Class I
    Active 510(k) 510(k) I
  • Forceps #101 And #102 Ref K790854

    Class I
    Active 510(k) 510(k) I
  • Proctoscope #501 Ref K790856

    Class II
    Active 510(k) 510(k) II
  • Easy-Spec Ref K790853

    Class II
    Active 510(k) 510(k) II
  • Vagi-Spec Ref K790852

    Class II
    Active 510(k) 510(k) II
  • Catheterization Forcep Ref K792494

    Class I
    Active 510(k) 510(k) I
  • Surgical Drape Clip #201 Ref K790855

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

Frequently asked questions

How many devices does C. Intl. have in the registry?

The registry currently lists 7 devices for C. Intl.. Devices recorded under merged duplicate company entries are counted once.

Which registries list C. Intl.'s devices?

Among its 7 most recently registered devices, C. Intl. has devices listed in FDA 510(k) (7 devices).

What risk classes do C. Intl.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for C. Intl.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from C. Intl. in the registry?

The most recently registered devices listed for C. Intl. include VAGI-PRESS #401, FORCEPS #101 AND #102, PROCTOSCOPE #501 and EASY-SPEC.

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