BEUDAMED
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    NASAL EASE ALLERGY BLOCKER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RC Screw-retained Abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600303510·

    CASTROVIEJO CORNEAL SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896014381·CASTROVIEJO CORNEAL SCISSORS MEDIUM CURVED BLUN...

    Integra®

    FDA UDI
    INTEGRA PAIN MANAGEMENT·10381780260462·ARTHROGRAM TRAY

    Bozemann Needle Holder

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896120488·Bozemann Needle Holder Tungsten Carbide Serrate...

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668103104·OBSTBAUM SYNECHIAE SPATULA

    Integra®

    FDA UDI
    INTEGRA PAIN MANAGEMENT·10381780429692·Arthrogram Tray

    ORTRAUTEK TRAUMA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    BD NEXIVA CLOSED IV CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124282·L Ultracongruent Tibial Insert Trial Sz C 20mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144693·L CR UHMWPE Ultracongruent Tibial Insert Sz C 20mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102068·L CR MAXTM HXL Ultracongruent Tibial Insert Sz ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101207·L CR E-MAXTM Vitamin E Ultracongruent Tibial In...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523164530·L Ultracongruent Tibial Insert Trial with Anter...

    UNKNOWN NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·October 1, 2014

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·May 29, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·February 19, 2026

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 9, 2022

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 30, 2026