BEUDAMED
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    Respire Pink Series-Herbst-EF

    FDA 510(k)
    FDA Class 2 ·Dental

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171028970·PESSARY, OVAL #4, W/O SUPPORT, 2.75"

    INTERACTIVE SBM 3.7MMDX13MML 3.0MM PLAT

    FDA Adverse Event
    Injury ·IMPLANT DIRECT SYBRON MANUFACT·Product code DZE·October 29, 2025

    VERSACLOSE, MODEL VC-200-01

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

    MAMMODIAGNOST DR

    FDA 510(k)
    FDA Class 2 ·Radiology

    PENUMBRA SMART COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015

    RINGLOC-X E1 H/W 56/32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 11, 2025

    ZIMMER REVERSE SHOULDER HUMERAL STEM

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSD·June 22, 2011

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 6, 2013

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008