13 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Implant Direct Dental Implant Systems Portfolio - MR Conditional
FDA 510(k)
FDA Class 2
·Dental
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113508·PS-C Insert, Size 2 x 11mm
BENCO
FDA UDI
BENCO DENTAL SUPPLY CO.·00366975004185·#30 Blue .02 Taper Benco Dental Gutta Percha Po...
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776299552·Suction Nerve Root Retractor, 7fr 6mm 8" Length
Steerable IBD
FDA UDI
Seaspine Orthopedics Corporation·10889981117337·Fixed Rasp; 22x11 (05-3301)
HLS UNI EVOLUTION PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
SYNTHES NAVIGABLE PEDICLE PREPARATION INSTRUMENTS
FDA 510(k)
FDA Class 2
·Neurology
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·September 3, 2024
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 15, 2010
NAVIGABLE HANDLE FOR USE WITH ACCESS CANNULA
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HAW·April 19, 2017
PULSE GEN MODEL 102
FDA Adverse Event
Death
·CYBERONICS, INC.·Product code LYJ·November 3, 2014
MAZE LINEAR CARDIAC PROBE
FDA Adverse Event
Malfunction
·ATRICURE, INC.·Product code GEH·August 24, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 12, 2013