BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    RITCH TRABECULOPLASTY LASER LENS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    K2-HF Dentine Modifier (Orange) MM-OR 20g.

    FDA UDI
    Yeti Dentalprodukte GmbH·EYET38625120·

    Shoreline™ ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981177508·Modular Trial, 14 x 13 x 12mm, 15 Deg Lordosis

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867125599·HEADLESS COMPRES SCRW 2.5X12MM

    REPCO EASY-BREATHER CLINICAL AIR PUMP

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    truSculpt

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    G7 NEUTRAL E1 LINER 36MM D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·March 13, 2018

    G7 PPS LTD ACET SHELL 50D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·March 13, 2018

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    UNIV-FEMNAIL Ø10 L380 SST

    FDA Adverse Event
    Injury ·SYNTHES·Product code JDS·December 10, 2012

    ISOFLEX OPTIM LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·June 23, 2015

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020