21 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRIMACONNEX INTERNAL CONNECTION IMPLANT SYSTEM, PRIMACONNEX INTERNAL CONNECTION PROSTHETICS
FDA 510(k)
FDA Class 2
·Dental
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788020154·RX Coudé® Epidural Needle 14g TW x 6.0"
LEONE SPA
FDA UDI
LEONE SPA·08033707000020·ASYMMETRIC FAN-TYPE SCREW S/STEEL 15mm
PRACTICON, INC.
FDA registration
PRACTICON, INC.·37 products·🇺🇸 United States
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B1675051614070·
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B1675051614000·
TALOS®-C
FDA UDI
SpineArt SA·07640375236869·NON-STERILE TALOS®-C PLANAR MODULAR TRIAL
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B167505161407A0·
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B167505161400A0·
STRYKER TRAUMA PELVIC SET
FDA 510(k)
FDA Class 2
·Orthopedic
DIGITAL CLINICAL THERMOMETER, MODEL ACT 3020
FDA 510(k)
FDA Class 2
·General Hospital
SUBDURAL TUNNELING KIT
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES·Product code HCA·March 15, 2007
SUBDURAL TUNNELING KIT
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES·Product code GWM·March 15, 2007
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 4, 2025
TALOS®-C
FDA UDI
SpineArt SA·07640375237194·NON-STERILE TALOS®-C CONVEX MODULAR TRIAL
BROACH, PEGGED GLENOID
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·April 10, 2024
BROACH, PEGGED GLENOID
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·April 10, 2024
BROACH, PEGGED GLENOID
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·March 14, 2022
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·September 2, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·April 12, 2011