19 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Bioabsorbable Anchor
FDA 510(k)
FDA Class 2
·Orthopedic
INDUS TEXTILES TOWEL-STERILE AND NON-STERILE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
JIAJIAN POINTOSELECT DIGITAL
FDA 510(k)
FDA Class 2
·Neurology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 7, 2025
TUBE, GASTROINTESTINAL (AND ACCESS)
FDA Adverse Event
Injury
·C. R. BARD INC. (BASD)·Product code KNT·October 28, 2008
ECHELON*FLEX60 ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60 MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 17, 2011
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 9, 2013
DEKA SMARTPERIO
FDA Adverse Event
Injury
·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code NVK·December 11, 2024
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·January 12, 2022
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Pulse Generator
FDA Enforcement
Class II
·Ongoing·Boston Scientific Corporation·September 25, 2019