77 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATTUNE FEMORAL INTRODUCER
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code HWA·December 11, 2018
Sparkle Prophylaxis Paste
FDA UDI
CROSSTEX INTERNATIONAL, INC.·10732224001965·Prophylaxis Paste with Xylitol, Assorted flavor...
Sparkle Prophylaxis Paste
FDA UDI
CROSSTEX INTERNATIONAL, INC.·10732224002023·Prophylaxis Paste with Xylitol, Assorted flavor...
EYEWEAR BY ROI PUYA GOLD
FDA UDI
Eyewear By Roi, Limited·00748474331526·52-16-140 GOLD KAREN KANE
EYEWEAR BY ROI PUYA GOLD
FDA UDI
Eyewear By Roi, Limited·07484743315264·52-16-140 GOLD KAREN KANE
ARROW
FDA UDI
TELEFLEX INCORPORATED·00801902091543·Percutaneous Sheath Introducer Kit with Integra...
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902118186·PSI Kit for use with 7.5 - 8 Fr. Catheters
Superflex Kids Collection
FDA UDI
WestGroupe Optical Inc·00676190682977·Spectacle Frame
Superflex Kids Collection
FDA UDI
WestGroupe Optical Inc·00676190682939·Spectacle Frame
POLYMEDIC UPA NERVE STIMULATION NEEDLE; POLYMEDIC UPC NERVE STIMULATION NEEDLE
FDA 510(k)
FDA Class 2
·Neurology
NO 4. TRIATHLON TS PLUS TIBIAL INSERT X3 POLY 22MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·October 27, 2016
ARTHRO TISSLIB BLADE UP *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code NBH·May 21, 2020
ARTHRO TISSLIB BLADE UP *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code NBH·January 30, 2019
ARTHRO TISSLIB ATRAUMATIC UP *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code NBH·December 10, 2024
ARTHRO TISSLIB BLADE UP *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code NBH·September 5, 2018
Obsidio Conformable Embolic, Material Numbers (UPN): a) M0013972001010, b) M0013972101010
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code KRD·February 20, 2024
Obsidio Conformable Embolic, Material Numbers (UPN): a) M0013972001010, b) M0013972101010
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·April 3, 2024
ARTHRO GRASPER PEN 35 UP *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code NBH·June 1, 2022
ARTHRO GRASPER PEN 35 UP *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code NBH·September 30, 2025
ARTHRO GRASPER PEN 35 UP *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code NBH·September 30, 2020