10 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CarboClear® Hybrid Pedicle Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113813·VISCO CANNULA 27GA ANGLE 8MM
Portex
FDA UDI
ICU MEDICAL, INC.·15019517072792·
VEGA Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
PINN-ACL CROSSPIN
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM FOLLOW APP
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·September 2, 2025
PEN NEEDLE 32GX4MM 5B 28CT
FDA Adverse Event
Malfunction
·EMBECTA MEDICAL DEVICES (SUZHOU) CO., LTD., CHINA·Product code FMI·February 18, 2025
ATLAS DR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2011
PINNACLE SECTOR II CUP 52MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·November 21, 2008
TALENT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·July 23, 2013