34 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Biofourmis Everion+ (G2)
FDA 510(k)
FDA Class 2
·Cardiovascular
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551082232·Micro Elevator, 0.7 mm, right, 18 cm
ELMED
FDA UDI
ELMED INCORPORATED·00842180148505·Extra Deep Hip Retractor, [Extra Deep Mueller-t...
INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TSX-101A/A AND TSX-101A/C AQUILION MULTISLICE CT SCANNERS
FDA 510(k)
FDA Class 2
·Radiology
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 3, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 20, 2025
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 21, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 12, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
UNKNOWN DEPUY ASR SLEEVE
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWY·November 6, 2014
E1 VANGUARD TIBIAL BEARING 10MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·September 2, 2011
SABINA
FDA Adverse Event
Malfunction
·LIKO AB·Product code FSA·July 11, 2013
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 26, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 20, 2025
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 2, 2024