30 results · 27ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

IV-eye

FDA 510(k)
FDA Class 1 ·General Hospital

MERIT ONE SNARE SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFT

FDA 510(k)
FDA Class 2 ·Physical Medicine

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

CAPSURE SP NOVUS

FDA Adverse Event
Injury ·MPRI·Product code DTB·June 7, 2013

IVT DISPOSABLE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MALTA·Product code KPE·July 7, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 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

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·July 19, 2019

PTA BALLOON CATHETER(OHICHO3)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·December 13, 2017