10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Powder Free Vinyl Patient Examination Gloves
FDA 510(k)
FDA Class 1
·General Hospital
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180522158·4mm KERRISON 90 DEG. BAYONETED, W/O Tang
STRYKER SPINE AVS TL PEEK SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
XL EXTRACTION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
URETEX TO2 URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·SOFRADIM PRODUCTIOJN·Product code OTN·April 11, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 26, 2014
ILS CURVED CIR STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 28, 2011
UNKNOWN HIP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·December 12, 2014
MALIBU
FDA Adverse Event
Injury
·SEASPINE INC.·Product code NKB·February 12, 2020
MALIBU
FDA Adverse Event
Injury
·SEASPINE INC.·Product code NKB·February 12, 2020