Ecleris
US Last updated 24 May 2026
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- Devices
- 153
- Registries
- GUDIDEUDAMEDFDA
- FDA recalls
- 0
Catalogue
Portaled R00 Ref R00
Portaled RX1 Ref RX1
Procam 4K R00 Ref R00
Procam 4K Usb RX1 Ref RX1
Procam HD CMOS II R04 Ref R04
Procam 4K R00 Ref R00
Microscope R02 Ref R02
Sinuscope R00 Ref R00
Procam Pack RX1 Ref RX1
LaryngoPro R00 Ref R00
Sinuscope R00 Ref R00
Everlux R02 Ref R02
Sinuscope R00 Ref R00
Sinuscope R00 Ref R00
Laringoscope R00 Ref R00
Procam HD II RX1 Ref RX1
Procam Hd 2D R00 Ref R00
Minivac R02 Ref R02
Everlux Mini R00 Ref R00
Laringoscope R00 Ref R00
Microscope RX1 Ref RX1
Sinuscope R00 Ref R00
MICROSTAR Colposcope R01 Ref R01
Microscope R00 Ref R00
Microscope RX1 Ref RX1
Procam Sd R00 Ref R00
Microscope RX1 Ref RX1
Sinuscope R00 Ref R00
MICROSCOPE Colposcope RX1 Ref RX1
Fns-2800 RX1 Ref RX1
Microscope RX1 Ref RX1
Microscope R00 Ref R00
Sinuscope R00 Ref R00
Sinuscope R00 Ref R00
MICROSCOPE Colposcope R00 Ref R00
Everlux Pro R00 Ref R00
Microscope RX1 Ref RX1
MICROSCOPE Colposcope R00 Ref R00
Microscope R00 Ref R00
Microscope RX1 Ref RX1
Vng 3D R00 Ref R00
MICROSCOPE Colposcope RX1 Ref RX1
Otoscope R00 Ref R00
Microscope RX1 Ref RX1
Microscope R01 Ref R01
Microscope RX1 Ref RX1
Microscope R00 Ref R00
Sinuscope R00 Ref R00
Sinuscope R00 Ref R00
Everlux R02 Ref R02
Showing 1-50 of 153
FDA establishments
- 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.
Information
- Country
- US
- Website
- ecleris.com
- [email protected]
- Phone
- 786-483-7490
- DUNS number
- 043555079