30 results · 23ms · Sources: EU EUDAMED, US FDA

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3Shape Ortho System

FDA 510(k)
FDA Class 2 ·Dental

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704283532·LAHEY FINGER RETRACTOR 4 3/4" 2 PRONG SHARP

ENCORE REVERSE SHOULDER PROSTHESIS HUMERAL STEM ADAPTER

FDA 510(k)
FDA Class 2 ·Orthopedic

ELECSYS CA 125 II CALCHECK 5

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

COLLEAGUE PRE P1.7

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

RIA DRIVESHAFT L520

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HTO·June 7, 2013

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

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

AMISTEM H STEM SIZE 4 STD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 29, 2016

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