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    COR HEALTH, INC

    FDA registration
    COR HEALTH, INC·2 products·🇺🇸 United States

    CORTRAK ENTERAL ACCESS SYSTEM - RECEIVER UNIT

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·August 13, 2019

    VITROS 3600 IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Injury ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JJE·February 16, 2024

    COULTER AC*T 5 DIFF ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·May 12, 2011

    COATED VICRYL

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·April 3, 2026

    SUREFORM

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code GDW·June 8, 2022

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, right, 19 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-021-19. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 11 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-11. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 9 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-09. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 13 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-13. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, right, 16 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-021-16. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1 or 2, right, 9 MM height, for use with baseplate size 1, 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-021-09. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, left, 13 MM height, for use with baseplate size 1 or 2 sterile, Zimmer, Warsaw, IN; REF 00-5424-011-13. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, right, 16 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-021-16. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, left, 11 MM height, use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-011-11. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, right, 19 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-021-19. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, left, 19 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-011-19. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, left, 9 MM height, use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-011-09. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, ultracongruent, Size 1,2, right, 11 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5428-021-11. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009

    Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 1,2, right, 11 MM height, for use with baseplate size 1 or 2, sterile, Zimmer, Warsaw, IN; REF 00-5424-021-11. The device is a semiconstrained total knee prosthesis components indicated for uncemented or cemented use in skeletally mature individuals.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 8, 2009