7 results
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26ms
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Sources: EU EUDAMED, US FDA
NEUROLOGICAL SCREENING STIMULATOR M 3623
FDA 510(k)
FDA Class 2
·Neurology
AVS PL PEEK SPACERS, MODELS 48351 AND 48353
FDA 510(k)
FDA Class 2
·Orthopedic
Osteocera Resorbable Bone Substitute
FDA 510(k)
FDA Class 2
·Orthopedic
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 30, 2014
ESPRIT
FDA Adverse Event
Injury
·SORIN CRM S.R.L.·Product code NVZ·October 5, 2012
MULTIFIRE ENDO GIA 30-2.5 (V) 12MM STAPLE
FDA Adverse Event
Injury
·USSC PUERTO RICO·Product code GDW·July 27, 2010
Pinnacle Cups, Part numbers 121701048 121701050 121701052 121701054 121701056 121701058 121701060 121701062 121711048 121711052 121712050 121712052 121712056 121722048 121722050 121722052 121722054 121722056 121722058 121722060 121722062 121731048 121731050 121731052 121731054 121731056 121731058 121731060 121731062 121732048 121732050 121732052 121732054 121732056 121732058 121732060 121732062 121732064 - Product Usage: The PINNACLE CUP devices are part of the Pinnacle Hip Solution for the anatomic reconstruction of the hip joint, which promotes prosthetic joint load and function.
FDA Enforcement
Class II
·Terminated·DePuy Orthopaedics, Inc.·January 13, 2021