BEUDAMED
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    PLASMALIPO/PLASMA D30 LSER SURGICAL DEVICE

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

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120274·Guidewire 0.9x100mm Dbl Trocar

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120281·Guidewire 0.9x100mm Sgl Trocar Gold Tip

    MATHIEU NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896046009·MATHIEU NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED...

    PHYSICA FIXED TIBIAL PLATE #2

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JWH·March 8, 2023

    PHYSICA KNEE - FIXED TIBIAL PLATE CEMENTED #9

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JWH·November 27, 2023

    BIPAP AUTO BIFLEX

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·January 12, 2026

    MODIFICATION TO CAVERMAP SURGICAL AID

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    SOFTLINE SPRING CLIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 28, 2025

    SMR SHOULDER

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·April 30, 2025

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 29, 2013

    MITEK EXPRESSEW III NEEDLE

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code LXH·September 18, 2014

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·May 16, 2011

    BIOLOX DELTA CER LNR 36MM G

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 12, 2022

    IMP,TSV,6.0,8,MTX,MG

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·January 10, 2023

    IMP,TSV,4.7,10,MTX,MG

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·January 10, 2023

    SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098

    FDA Recall
    Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code EWO·September 26, 2023

    SENTIERO Screening2, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S2

    FDA Recall
    Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code EWO·September 26, 2023

    SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S

    FDA Recall
    Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code EWO·September 26, 2023