8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BEAM BLOCK TRAYS
FDA 510(k)
FDA Class 2
·Radiology
CAPSTONE® L Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169133181·CAGE 2964840 CAPSTONE-L 6 DEG 8X40
DERMAPROOF
FDA 510(k)
FDA Unclassified
·Unknown
ORION PLUS/MODIFICATION
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·February 15, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011
UNIDENTIFIED SIZE 4 CR POROCOAT FEMUR
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 29, 2014
BIOMET StageOne Knee Tibial Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 433170.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020