Corcym Inc.

FDA Device Registration & Listing · Englewood, CO, US · Registration 3019892983

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3019892983
FEI Number
3019892983
Entity Name
Corcym Inc.
City/State/Country
Englewood, CO, US
Establishment Address
9800 Mount Pyramid Court, Suite #400, Englewood, CO 80112, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Corcym S.r.l. (Owner Number: 9083203)
Owner / Operator Contact Address
Via Crescentino sn, Saluggia, IT-VC 13040, IT
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K163608
PMA Number
N/A

All Registered Proprietary Names

HAART 200 Aortic Annuloplasty Device and accessories HAART 300 Aortic Annuloplasty Device and accessories

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PST Aortic Annuloplasty Ring Cardiovascular Class 2 870.3800 2023-11-30
PST Aortic Annuloplasty Ring Cardiovascular Class 2 870.3800 2023-11-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Corcym S.r.l.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005687633 Corcym S.r.l. SALUGGIA Vercelli, IT

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019892983. Last updated year: 2026. Please use registration number 3019892983 when referencing this establishment in official correspondence.
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