8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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8ch Knee-Foot SPEEDER
FDA 510(k)
FDA Class 2
·Radiology
BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304254510·
TOP NEUROPOLE NEEDLES, MODELS ST, X, RC, XE AND TL
FDA 510(k)
FDA Class 2
·Neurology
CORELEADER COLLA-PAD MODEL CS 03030
FDA 510(k)
FDA Unclassified
·Unknown
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 9, 2024
SPRINT
FDA Adverse Event
Injury
·MPRI·Product code LWS·October 10, 2014
SOLETRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·June 11, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·July 15, 2011