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    Corcym Inc.

    FDA registration
    Corcym Inc.·1 product·🇺🇸 United States

    HAART

    FDA UDI
    Corcym Inc.·10857160006260·Aortic Annuloplasty Device

    HAART

    FDA UDI
    Corcym Inc.·10857160006239·Aortic Annuloplasty Ring

    HAART

    FDA UDI
    Corcym Inc.·10857160006307·Aortic Annuloplasty Ring

    HAART

    FDA UDI
    Corcym Inc.·10857160006291·Aortic Annuloplasty Ring

    HAART

    FDA UDI
    Corcym Inc.·10857160006284·Aortic Annuloplasty Device

    HAART

    FDA UDI
    Corcym Inc.·10857160006253·Aortic Annuloplasty Device

    HAART

    FDA UDI
    Corcym Inc.·10857160006246·Aortic Annuloplasty Device

    HAART Polyester Pledget 6-Pack

    FDA UDI
    Corcym Inc.·10857160006338·Polyester pledgets for use with HAART Aortic An...

    HAART

    FDA UDI
    Corcym Inc.·10857160006277·Aortic Annuloplasty Ring

    HAART

    FDA UDI
    Corcym Inc.·10857160006314·HAART 301 Instrument Set (handles and sizers)

    HAART 300 AORTIC ANNULOPLASTY DEVICE

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·October 17, 2025

    HAART 200 AORTIC ANNULOPLASTY DEVICE

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·December 4, 2025

    HAART 200 AORTIC ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·May 9, 2025

    HAART 200 AORTIC ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·May 8, 2025

    HAART 200 AORTIC ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·May 9, 2025

    HAART 200 AORTIC ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·May 9, 2025

    HAART 200 AORTIC ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·May 9, 2025

    HAART 200 AORTIC ANNULOPLASTY DEVICE

    FDA Adverse Event
    Injury ·BIOSTABLE·Product code KRH·March 2, 2024

    HAART AORTIC ANNULOPLASTY DEVICE

    FDA Adverse Event
    Injury ·BIOSTABLE·Product code KRH·June 19, 2024