24 results · 25ms · 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.

Wrist Pulse Oximeter

FDA 510(k)
FDA Class 2 ·Cardiovascular

GRAND WORK PLASTIC PRODUCTS CO., LTD. POWDER FREE VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

XR-SERIES BI-METRIC FEMORAL COMPONENTS

FDA 510(k)
FDA Class 2 ·Orthopedic

SPRINT FIDELIS

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

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

IMTEC

FDA Adverse Event
Injury ·IMTEC·Product code DZE·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

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

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

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

OHICHO NEO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 31, 2025

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·May 28, 2020

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2018

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 7, 2018