27 results · 31ms · Sources: EU EUDAMED, US FDA

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Reprocessed Steerable Introducer

FDA 510(k)
FDA Class 2 ·Cardiovascular

Epredia

FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063791·The blades and knifes consumables are for use w...

LEONE SPA

FDA UDI
LEONE SPA·08033707014171·CALIBRA 1ST MOL BANDS W/G8325-02 KIT UR

SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

SPLASH! IMPRESSION MATERIAL DEVICE

FDA 510(k)
FDA Class 2 ·Dental

QUADRA H CEMENTLESS STEM SIZE 3 LAT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·November 25, 2015

CERVSPINE-EXP-HEADSCR 4 SELF-DRILL L14

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code KWQ·October 8, 2014

PROTECTA XT CRT-D

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 7, 2013

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·July 7, 2011

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

HYBRID GLENOID BASE SMALL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 8, 2018

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