28 results
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44ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Mosie Baby Kit
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Lumipulse G Specimen Diluent 1
FDA UDI
FUJIREBIO INC.·04987270231203·
ELMED
FDA UDI
ELMED INCORPORATED·00842180161009·PRISM CERVICAL CURETTE 10" ANGLED 90° 1, ORANGE
Sklar®
FDA UDI
SKLAR CORPORATION·10649111153969·SKLARLITEXD LISTER BAND 7.25"
S³MODULAR QK CONNECT HANDLE LARGE
FDA UDI
Biomet Orthopedics, LLC·00887868025600·
S3™PLATE TRIAL - LEFT
FDA UDI
Biomet Orthopedics, LLC·00887868025747·
S³™STERILE TRAY
FDA UDI
Biomet Orthopedics, LLC·00887868025730·
S3™PLATE TRIAL - LEFT
FDA UDI
Biomet Orthopedics, LLC·00887868025754·
BIAX A.F. WRIST/BIAX ADVANCED FIXATION WRIST
FDA 510(k)
FDA Class 2
·Orthopedic
IHEALTH CLOUD
FDA 510(k)
FDA Class 2
·Cardiovascular
COCHLEAR OSIA OSI300 IMPLANT
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code PFO·March 8, 2026
COCHLEAR OSIA OSI300 IMPLANT
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code PFO·January 15, 2024
COCHLEAR OSIA OSI300 IMPLANT
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code PFO·January 15, 2024
ETS FLEX ARTICING LNR CUTR 45MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 10, 2008
WAVELIGHT FS200 FEMTOSECOND LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code GEX·August 25, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·July 17, 2013
CARTO 3
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·September 16, 2024
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·May 21, 2024
CARTO 3
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·October 28, 2025
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·April 17, 2024