10 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PSP TEMP - TRAY
FDA 510(k)
FDA Class 1
·Dental
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209116775·
Legacy™ GPS® Abutment
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307111276·
FIRMap Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
KALIX II IMPLANT, MODEL 141 0XX WITH XX
FDA 510(k)
FDA Class 2
·Orthopedic
VDW SILVER RECIPROCATING MOTOR
FDA Adverse Event
Malfunction
·DENTSPLY VDW GMBH·Product code EBW·August 14, 2019
VDW SILVER RECIPROCATING MOTOR
FDA Adverse Event
Malfunction
·DENTSPLY VDW GMBH·Product code EBW·August 7, 2020
UNIVERSAL STEM 75X16MM FLUTED
FDA Adverse Event
Injury
·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code JWH·June 6, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code MDS·October 5, 2010
MYNX CADENCE VASCULAR CLOSURE DEVICE 6/7F
FDA Adverse Event
Injury
·ACCESSCLOSURE, INC.·Product code MGB·July 2, 2012