76 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·November 19, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·November 19, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·November 19, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·November 19, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·November 20, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·April 9, 2024
MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·November 19, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Malfunction
·MOXIMED, INC.·Product code QVV·September 9, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Injury
·MOXIMED, INC.·Product code QVV·July 17, 2024
MISHA KNEE SYSTEM
FDA Adverse Event
Malfunction
·MOXIMED, INC.·Product code QVV·November 8, 2024
MISHA KNEE SYSTEM
FDA Adverse Event
Malfunction
·MOXIMED, INC.·Product code QVV·April 2, 2025
MISHA KNEE SYSTEM
FDA Adverse Event
Malfunction
·MOXIMED, INC.·Product code QVV·January 31, 2025
MISHA® KNEE SYSTEM, SMALL, RIGHT
FDA Adverse Event
Malfunction
·MOXIMED, INC.·Product code QVV·January 20, 2026
MISHA KNEE SYSTEM
FDA Adverse Event
Malfunction
·MOXIMED, INC.·Product code QVV·February 7, 2025
MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: 2-1002.
FDA Recall
Open, Classified
·Moximed, Inc.·Product code QVV·December 2, 2024
Medial Knee Implanted Shock Absorber
FDA classification
FDA Class 2
·Medial Knee Implanted Shock Absorber
Neobiotech Implant System
FDA UDI
Neobiotech. co., ltd·08809276763129·Ø3.5
LVV OPTION
FDA 510(k)
FDA Class 2
·Cardiovascular
Front load bipolar electrode
FDA UDI
CHIRURGIE INNOVATION·03760263240052·(Fr26)
DV TEST AND DVV CONFIRM
FDA 510(k)
FDA Class 1
·Hematology