21 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Anatomical Shoulder System/Anatomical Shoulder Domelock System/Anatomical Shoulder Fracture System
FDA 510(k)
FDA Class 2
·Orthopedic
OsteoMed
FDA UDI
OSTEOMED LLC·00845694026574·MFx Angulated Locking Fracture Plate, 4 Hole, 37mm
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023609·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023586·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
Perfect Fit
FDA UDI
DYMEDIX DIAGNOSTICS, INC.·00817377020469·Perfect Fit ™II Adult Effort Belt Sensor, Abdom...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023616·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023593·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023555·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023579·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023623·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023562·Ø14MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...
MIRAGE SWIFT
FDA 510(k)
FDA Class 2
·Anesthesiology
SAM CHEST SEAL WITH VAVLE; SAM CHEST SEAL
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180522097·PROBE SHIELD, 100 MM
LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016
LIFEPAK(R) 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015
LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014
PELVICOL ACELLULAR COLLAGEN MATRIX
FDA Adverse Event
Injury
·TISSUE SCIENCE LABORATORIES·Product code FTL·April 26, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·June 21, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 3, 2008