22 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PMT Posterior Cervical Stabilization System (PCSS)
FDA 510(k)
FDA Unclassified
·Unknown
REMEL
FDA UDI
REMEL, INC.·00848838026560·CandidaTube (BiGGY Agar) PK/10
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017972·K-Wire, Single Ended, Trocar Point, Diameter Si...
Zimmer
FDA UDI
Provision·B504OM2410350·
Zimmer
FDA UDI
Provision·00810041638045·
NA
FDA UDI
Zimmer, Inc.·00889024062214·
NA
FDA UDI
STERILMED, INC.·10888551021654·DRILL BIT TWIST
Mui Scientific
FDA UDI
H & A Mui Enterprises Inc·10678467507010·24-Channel Customized Single-Use HRM Anorectal ...
Portex
FDA UDI
ICU MEDICAL, INC.·15019517070217·
HOFFRICHTER TREND 110 CPAP DEVICE WITH AQUATREND III CPAP HUMIDIFIER ACCESSORY FOR TREND
FDA 510(k)
FDA Class 2
·Anesthesiology
ETHICON Linx Esophagus Sizing Tool
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
M.U.S.T. PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PML·February 26, 2026
CARDINAL HEALTH
FDA Adverse Event
Malfunction
·CARDINAL HEALTH 200, LLC·Product code GBX·March 3, 2026
PINNACLE SECTOR II CUP 54MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·November 19, 2008
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·August 10, 2011
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 18, 2013
M.U.S.T. PEDICLE SCREW SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code PML·November 13, 2025
BELLATEK HYBRID BAR 4 IMPLANTS
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·December 26, 2024
BELLATEK HYBRID BAR 4 IMPLANTS
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·January 6, 2025
BELLATEK¿ HYBRID BAR 5 IMPLANTS
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·February 18, 2025