Horizons Intl. Corp.
US Last updated 23 May 2026
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- Devices
- 10
- Registries
- FDA 510(k)FDA
- FDA recalls
- 0
Catalogue
Horizons International Varices Injection Needles Ref K010448
Horizons Cytology Brush Ref K021998
Horizons Papillotome Ref K002236
Horizons Reusable Hot Biopsy Forceps Ref K022243
Tornado Rotatabel Snare And Polyp Catcher Ref K083049
Horizons Hot Biopsy Forceps Ref K021706
Horizons Reusable Polypectomy Snares Ref K022268
Horizons Anso Transbronchial Aspiration Needles Ref K022546
Horizons International Polypectomy Snares Ref K011667
Horizons Ercp Cannula Ref K002235
FDA establishments
- Horizons Intl. Corp. HEREDIA · CR FEI 3004083736
What Horizons Intl. Corp. makes
Horizons Intl. Corp. manufactures medical devices including cytology brushes, papillotomes, reusable hot biopsy forceps, rotatable snares, polyp catchers, transbronchial aspiration needles, polypectomy snares, and ERCP cannula.
The company's portfolio consists of Class II devices listed in the FDA 510(k) registry, and Horizons Intl. Corp. is based in the US.
Frequently asked questions
What medical devices does Horizons Intl. Corp. manufacture?
Horizons Intl. Corp. produces Class II medical devices including cytology brushes, papillotomes, reusable hot biopsy forceps, rotatable snares, polyp catchers, transbronchial aspiration needles, polypectomy snares, and ERCP cannula.
Where is Horizons Intl. Corp. based?
Horizons Intl. Corp. is based in the United States, as indicated in the device registry information.
Which regulatory registries list Horizons Intl. Corp.'s devices?
Horizons Intl. Corp.'s devices are listed in the FDA 510(k) registry, which is a premarket notification database for medical devices in the United States.
How are Horizons Intl. Corp.'s devices classified?
All of Horizons Intl. Corp.'s devices are classified as Class II medical devices, which require general controls and special controls to ensure their safety and effectiveness.
Information
- Country
- US