21 results · 22ms · Sources: EU EUDAMED, 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