BEUDAMED
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    Zimmer® Natural Nail® System Cephalomedullary Nails; Affixus® Natural Nail® Humeral Nail System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111141164·SKLARLITE-XD OP SCIS SS ST 5.5

    DIGITAL FLAT PANEL X-RAY DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172382·CR Tibial Insert Trial with Posterior Pin Relie...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101412·R CR E-MAXTM Vitamin E Congruent Tibial Insert ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124428·R CR Tibial Insert Trial Sz A 14mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102181·R CR MAXTM HXL Congruent Tibial Insert Sz A 14mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523165599·R CR Tibial Insert Trial with Anterior Slot, Sz...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523145089·R CR UHMWPE Congruent Tibial Insert Sz A 14mm

    CARE TOUCH

    FDA Adverse Event
    Injury ·TIANJIN EMPECS MEDICAL DEVICE CO., LTD.·Product code NBW·April 12, 2023

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 11, 2008

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LGW·August 26, 2011

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 12, 2013

    VISIGLIDE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code OCY·November 25, 2024

    SKINTACT

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code GEI·April 16, 2024

    ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026