36 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RTVue XR OCT Avanti with AngioVue Software
FDA 510(k)
FDA Class 2
·Ophthalmic
Drill Extender
FDA UDI
BIO CONCEPT Co., Ltd.·06947600304340·
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100271·SAUER INFANT SPECULUM
ALBOGRAFT VASCULAR PROSTHESIS
FDA 510(k)
FDA Class 2
·Cardiovascular
GRAFTCAGE ACX
FDA 510(k)
FDA Class 2
·Orthopedic
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·February 19, 2025
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 20, 2025
CAPSUREFIX NOVUS MRI
FDA Adverse Event
Injury
·MPRI·Product code NVN·June 8, 2013
UNKNOWN DEPUY SZ5 MBT TIBIAL TRAY
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 28, 2011
PT2 GUIDE WIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·September 8, 2008
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·December 26, 2019
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
AXIOS?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024