34 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE
FDA 510(k)
FDA Class 2
·Immunology
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221046246·Unitek(TM) Molar Band General Purpose Wide Hard...
CAP 7.0MM MTP RESURFACING HEMI-ARTHROPLASTY
FDA 510(k)
FDA Class 2
·Orthopedic
RT200
FDA 510(k)
FDA Class 2
·Neurology
KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·March 17, 2020
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 25, 2025
GYNECARE TVT SECUR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code PAH·June 11, 2013
UNKNOWN DEPUY ASR CUP
FDA Adverse Event
Injury
·DEPUY INTL, LTD·Product code KWA·July 8, 2011
3.5MM PUBLIC SYMPHYSIS PLATE
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code HRS·September 10, 2008
IKAZUCHI ZERO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·June 13, 2019
KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·August 19, 2019
IKAZUCHI ZERO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·August 20, 2019
KANEKA PTCA CATHETER CO-R7(IKAZUCHI ZERO)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·August 21, 2019
KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code LOX·April 14, 2022
KANEKA PTCA CATHETER CO-R8 (TASUKI)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·December 13, 2020
KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code LOX·December 21, 2020
KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code LOX·April 13, 2022
KANEKA PTCA CATHETER CO-R6 (RAIDEN3)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·June 6, 2025
KANEKA PTCA CATHETER ZINRAI
FDA Adverse Event
Death
·KANEKA CORPORATION·Product code LOX·February 3, 2025
ARCOS LATERAL TROCH BOLT 42MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·September 22, 2017