53 results · 22ms · Sources: EU EUDAMED, US FDA

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Procedure mask/Surgical mask/Face mask

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Vivid ZirDisc Zircon Zahn System

FDA UDI
PEARSON DENTAL SUPPLIES, INC.·D724Q2500821·95x20mm 03HT (Translucent)

ELMED

FDA UDI
ELMED INCORPORATED·00842180134775·5 MM DIA., 33 CM, LAP. MONOPOLAR "L" HOOK ELECT...

ceraMotion®

FDA UDI
DENTAURUM GmbH & Co.KG·J011250082200·ceraMotion® Zr Shoulder B, 20 g / dental cerami...

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NQW·August 10, 2017

Panorama Patient Monitoring Network

FDA 510(k)
FDA Class 2 ·Cardiovascular

CENTERPIECE PLATE FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CENTERPIECE? PLATE FIXATION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code NQW·April 16, 2015

STYLE 68 SALINE FILLED BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FWM·May 6, 2025

CENTERPIECE¿ PLATE FIXATION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·June 8, 2016

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·December 7, 2017

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·June 11, 2020

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NQW·March 1, 2018

CENTERPIECE PLATE FIXATION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·February 22, 2018

DEPTH GAUGE FOR 2.0MM AND 2.4MM SCREWS

FDA Adverse Event
Malfunction ·SYNTHES JENNERSVILLE·Product code HTJ·November 14, 2014

ASR ACETABULAR IMPLANT 56

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·September 15, 2011