8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SILICONE COATED GUIDEWIRES
FDA 510(k)
FDA Class 2
·Cardiovascular
LACTOSCREW
FDA UDI
Biomet Orthopedics, LLC·00880304453401·
DANNIFLEX CPM 880(TM)
FDA 510(k)
FDA Class 1
·Physical Medicine
GSB ELBOW
FDA 510(k)
FDA Class 2
·Orthopedic
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 28, 2014
AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code FNL·January 9, 2013
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·November 19, 2010
REF 905581, 6.8 mm Lactoscrew 2#2 MB wI NDL, (Lactosorb L-15 resorbable copolymer ) Sterile, EO; Biomet Sports Medicine, Warsaw, IN Product Usage: The Biomet Sports Medicine Soft Tissue Anchoring Devices are resorbable repair devices used to attach soft tissue to bone.
FDA Recall
Terminated
·Biomet, Inc.·Product code HWC·January 25, 2012