36 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TETRIC EVOFLOW BULK FILL
FDA 510(k)
FDA Class 2
·Dental
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699557·GENUMEDI PSS BLUE SIZE III
AGXO
FDA UDI
Oticon A/S·05707131287762·H100V2, RITE 312 WL SIL AGXO
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304239210·
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962104538·ROUND BURR, 4.5MM, COMPATIBLE W/L
EKF- DIAGNOSTIC HEMO_CONTROL HEMOGLOBIN MEASUREMENT SYSTEM; EKF-DIAGNOSTIC HEMOGLOBIN MICROCUVETTES (MODIFIED CURVETTE W
FDA 510(k)
FDA Class 2
·Hematology
THE GUIDED SURGERY CONCEPT
FDA 510(k)
FDA Class 2
·Dental
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962102541·DISPOSABLE ARTHROSCOPIC 4.5mm ROUND BURR, COMPA...
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·February 2, 2018
ENDEAVOR RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·February 2, 2018
ENDEAVOR RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·February 2, 2018
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 6, 2013
OMEGA PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·July 6, 2011
RESTORE ADVANCED RECHARGEABLE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 5, 2008
ORTHOPEDIC SALVAGE SYSTEM NON-MODULAR LONG TIBIAL BASEPLATE 75MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·April 8, 2019
ORTHOPEDIC SALVAGE SYSTEM AXLE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·April 8, 2019
ORTHOPEDIC SALVAGE SYSTEM TIBIAL BEARING 12MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·April 8, 2019
ORTHOPEDIC SALVAGE SYSTEM TIBIAL BUSHING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·April 8, 2019
ORTHOPEDIC SALVAGE SYSTEM FEMORAL BUSHINGS SET
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·April 8, 2019
ORTHOPEDIC SALVAGE SYSTEM YOKE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·April 8, 2019