8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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M3 LAG SCREW FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110935·STERILIZING CASE NARROW
Solstice Occipito-Cervico-Thoracic System
FDA UDI
Life Spine, Inc.·00190837016982·
AMIA AUTOMATED PD SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AVANT GUARDIAN 101
FDA 510(k)
FDA Class 2
·General Hospital
TOTAL ASR ACET IMP SIZE 48
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·January 22, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·December 14, 2010
TENDRIL STS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014