8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EMA 3D
FDA 510(k)
FDA Class 2
·Dental
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668101193·FUKASAKU 'HOCKEY' KNIFE
SPECTRA QT: Q-SWITCHED ND: YAG LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AXIA RADIAL HEAD SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 21, 2025
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·November 14, 2008
SIGMA HP UNI INS 7MM LM/RL
FDA Adverse Event
Injury
·DEPUY RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code HRY·August 18, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 18, 2013