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Coroneo Inc

Canada·CA-MF-000019141

Last updated May 27, 2026

What Coroneo Inc makes

Coroneo Inc manufactures reusable surgical tools designed for cardiac and thoracic procedures, including sternum retractors of various sizes for adult, pediatric, and neonatal patients, as well as specialized atrial tissue retractors. Their portfolio also includes articulated arm systems for vascular access, aortic indexing cones, and universal clamps, alongside reusable medical rulers and retractors for general surgical retraction. These devices are engineered to assist in precise tissue exposure and stabilization during minimally invasive and open-heart surgeries.

The company’s devices are classified under EU and FDA regulatory frameworks, with products falling into Class I, Class IIa, and Class III categories depending on their risk level and intended use. Their devices are registered in the EU’s euamed database and the FDA’s UDI (Unique Device Identification) system, ensuring compliance with international medical device regulations. The manufacturer operates from Canada.

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

Frequently asked questions

What types of medical devices does Coroneo Inc manufacture?

Coroneo Inc specializes in reusable surgical tools primarily used in cardiac and thoracic procedures. Their product portfolio includes sternum retractors for adults, pediatric patients, and neonates, as well as specialized atrial tissue retractors. They also produce articulated arm systems for vascular access, aortic indexing cones, universal clamps, and reusable medical rulers and retractors for general surgical retraction. These devices are designed to aid in precise tissue exposure and stabilization during surgeries.

Where is Coroneo Inc based, and what regulatory databases list their devices?

Coroneo Inc is based in Canada. Their devices are registered in two key regulatory databases: the EU’s euamed system and the FDA’s UDI (Unique Device Identification) registry. These listings ensure compliance with international medical device regulations, though individual devices must undergo their own authorization processes.

How are Coroneo Inc’s devices classified under EU and FDA regulations?

Coroneo Inc’s devices are categorized based on risk and intended use, falling into Class I, Class IIa, and Class III under EU and FDA frameworks. Lower-risk items like reusable medical rulers typically qualify as Class I, while higher-risk devices—such as certain retractors or vascular systems—may be classified as Class IIa or Class III. Classification determines regulatory requirements, with higher classes requiring stricter pre-market evaluations.

Are Coroneo Inc’s devices used in pediatric or neonatal surgeries?

Yes, Coroneo Inc manufactures specialized devices tailored for pediatric and neonatal patients. Their portfolio includes pediatric sternum retractors for infants and neonates, as well as other tools designed to accommodate smaller anatomical structures during cardiac or thoracic procedures. These devices are engineered to ensure safe and effective use in vulnerable patient populations.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Canada
Address
9250, Avenue du Parc, Montreal, Canada
LinkedIn
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Facebook
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Phone
+1(514)336-9230
PRRC Contact
Valerio Valentini
EUDAMED SRN
CA-MF-000019141
FDA FEI Number
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DUNS Number
255276362

Catalogue (51)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Spreader arm - Neonate sternum retractor 1010835
EUDAMEDFDA UDI
Class IIaActive

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