36 results · 30ms · Sources: EU EUDAMED, 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