11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Natus Quantum
FDA 510(k)
FDA Class 2
·Neurology
SMITH & NEPHEW, INC. REVISION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EVEREST SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GUIDE SLEEVE F/HELICAL BLADE F/TFN
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code FZX·June 3, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·September 27, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 29, 2011
MLRY-HD POR FMRL 11X160MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWZ·June 26, 2019
M2A-MAGNUM PF CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·June 26, 2019
M2A-MAGNUM TPR INSRT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·June 26, 2019
LGN PRSFT STEM 10MMX220MM STRT
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·October 19, 2017
SOLARICE RX
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code LOX·August 26, 2019