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Ecleris

US Last updated 24 May 2026

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Devices
153
Registries
GUDIDEUDAMEDFDA
FDA recalls
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Catalogue153

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Registered with the FDA under this company group, matched by name.

  • Ecleris SRL Villa Martelli Buenos Aires · AR FEI 3005216736

What Ecleris makes

Ecleris manufactures optical and video-based medical imaging devices for surgical and diagnostic procedures, including general-purpose surgical microscopes, colposcopes, and rigid optical sinoscopes. Their portfolio also includes otoscopes, endoscopic otoscopes, rigid optical rhinolaryngoscopes, flexible video laryngoscopes, and surgical video cameras, often paired with general-purpose light sources for enhanced visualization. Specific products include systems like the Procam HD II and LaryngoPro, designed for procedures in otolaryngology, sinus surgery, and gynecology.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the United States, adhering to regulatory requirements for medical imaging equipment.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Website
ecleris.com
Phone
786-483-7490
DUNS number
043555079