18 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE
FDA 510(k)
FDA Class 1
·General Hospital
Tecomet
FDA UDI
TECOMET INC.·00841435109582·WIRE CUTTER FRONT SIDE, 15° ANGLE TC, WITH SAFE...
Tecomet
FDA UDI
TECOMET INC.·00841435124912·Wire Cutter
.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·April 30, 2025
.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·April 18, 2025
.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 21, 2025
ACE CANNULATED CORTICAL BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM
FDA 510(k)
FDA Class 1
·Clinical Chemistry
GYNECARE X-TRACT MORCELLATOR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code HET·June 8, 2006
.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·September 11, 2024
.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·November 19, 2024
.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·February 27, 2025
.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 18, 2025
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 19, 2016
UNKNOWN DEPUY ASR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·March 8, 2013
ENDURANT ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·February 11, 2011
SECURA DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·April 9, 2015