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    Arthrosurface, Inc.

    Manufacturer
    🇺🇸 United States

    ARTHROSURFACE, INC.

    FDA registration
    ARTHROSURFACE, INC.·18 products·🇺🇸 United States

    HEMICAP PATELLO-FEMORAL RESURFACING PROSTHESIS

    FDA Adverse Event
    ARTHROSURFACE·Product code KRR·November 16, 2015

    CARTIVA IMPLANT

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·February 25, 2022

    HEMICAP PATELLO-FEMORAL RESURFACING PROSTHESIS

    FDA Adverse Event
    Malfunction ·ARTHROSURFACE, INC.·Product code KRR·November 3, 2016

    HEMICAP/UNICAP RESURFACING PROSTHESIS

    FDA Adverse Event
    Other ·ARTHROSURFACE, INC.·Product code HSD·December 7, 2012

    ARTHROSURFACE TOEMOTION

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code LZJ·May 3, 2021

    HEMICAP® MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code KWD·December 26, 2017

    CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code KWD·October 17, 2017

    NANOFX PLEURISTIK

    FDA Adverse Event
    Malfunction ·ARTHROSURFACE, INC.·Product code LXH·December 15, 2017

    ARTHROSURFACE TOEMOTION

    FDA Adverse Event
    Malfunction ·ARTHROSURFACE, INC.·Product code LZJ·June 23, 2021

    PF WAVE IMPLANT UNICOMPARTMENTAL PATELLOFEMORAL JOINT - PRESS FIT 10 X 5 TROCHLE

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code KRR·December 13, 2021

    HEMICAP PATELLO-FEMORAL WAVE RESURFACING PROSTHESIS

    FDA Adverse Event
    Malfunction ·ARTHROSURFACE, INC.·Product code KRR·October 21, 2021

    GRS GLENOID RESURFACING SYSTEM

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code KWS·February 21, 2012

    NANOFX PLEURISTIK

    FDA Adverse Event
    Malfunction ·ARTHROSURFACE, INC.·Product code LXH·December 13, 2017

    HEMICAP® MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code KWD·October 25, 2017

    KISSIOC SUTURE SYSTEM

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code HTN·September 1, 2015

    NANOFX PLEURISTIK

    FDA Adverse Event
    Malfunction ·ARTHROSURFACE, INC.·Product code LXH·December 15, 2017

    HEMICAP

    FDA Adverse Event
    Injury ·ARTHROSURFACE, INC.·Product code KWD·April 14, 2026

    ARTHROSURFACE TOEMOTION

    FDA Adverse Event
    Malfunction ·ARTHROSURFACE, INC.·Product code LZJ·December 13, 2017