BEUDAMED
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    STAPIX SUPERELASTIC IMPLANT BONE STAPLES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AGXO

    FDA UDI
    Oticon A/S·05707131261632·H110, BTE 13 WL 100 DBL AGXO

    Segmental Plating System

    FDA UDI
    ALPHATEC SPINE, INC.·00190376545875·SPS FA Self-Tap Screw, 3.5 x 23 mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376695006·PROXIMITY FA SELF-TAP SCREW, 3.5 x 23mm

    K133532

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 2, 2021

    COLLAGEN-ORC ANTIMICROBIAL MATRIX

    FDA 510(k)
    FDA Unclassified ·Unknown

    185A+ TRANSPORT INCUBATOR WITH MASIMO PULSEOX, 185A+ TRANSPORT INCUBATOR WITH NELLCOR PULSEOX

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142972·L E-CIMA Vitamin E PS Tibial Insert Sz C 23mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147281·PS Tibia Insert Trial Size C, 23mm - Left

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144877·L UHMWPE PS Tibial Insert Sz C 23mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172856·PS Tibia Insert Trial with Posterior Pin Relief...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143832·L CIMA HXL PS Tibial Insert Sz C 23mm

    NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026

    INTERLOCK?-35

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code KRD·May 29, 2013

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 20, 2011

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAP·August 21, 2008

    PANEL PHOENIX NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026

    PANEL PHOENIX NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 23, 2026

    PANEL PHOENIX NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026

    PANEL PHOENIX NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026