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Corcym Inc.

Also registered as CORCYM SRL

United Statesfrom the FDA registration address FDA FEI 3019892983

Corcym Inc. is a medical device manufacturer, with 205 devices listed in FDA GUDID and EUDAMED (FDA Class III, II and I) as of 12 Nov 2026.

Devices
205
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 205
  • EUDAMED 49

A device listed in two registries counts in both.

Device classes
  • FDA Class III 90
  • FDA Class II 69
  • FDA Class I 38
Identifiers
  • FDA FEI 3019892983
  • DUNS 112833663

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Corcym Inc. makes

Corcym Inc. manufactures mechanical and self-expandable heart valve prostheses, including bi-leaflet aortic and mitral valves, as well as annuloplasty rings for open-surgery repair of the mitral and tricuspid valves. Their portfolio also includes reusable heart valve annulus sizers, single-use valve holders, and post-dilation balloon catheters for valve deployment. Some devices combine mechanical valves with biologic-polymer aorta grafts for aortic replacement.

The company’s products are regulated under FDA classifications, including Class I, Class II, and Class III devices, and are listed in the FDA’s Unique Device Identifier (UDI) database.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue205

Newest first, rows 1-50 of 205

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Rows 1-50 of 205

Showing 1-50 of 205

Company details

FDA FEI number
3019892983
DUNS number
112833663
Address
9800 Mount Pyramid Court, Suite #400, Englewood, CO, 80112
Phone
5129709112

Frequently asked questions

How many devices does Corcym Inc. have in the registry?

The registry currently lists 205 devices for Corcym Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Corcym Inc.'s devices?

Among its 50 most recently registered devices, Corcym Inc. has devices listed in EUDAMED (8 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Corcym Inc.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Corcym Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Corcym Inc. in the registry?

The most recently registered devices listed for Corcym Inc. include TriMemo TRIM-26, TriMemo TRIM-28, TriMemo TRIM-30 and TriMemo TRIM-32.

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