13 results · 20ms · 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.

LAVA ULTIMATE CAD/CAM RESTORATIVE FOR CEREC LAVA ULTIMATE CAD/CAM RESTORATIVE FOR E4D LAVA ULTIMATE IMPLANT CROWN RESTOR

FDA 510(k)
FDA Class 2 ·Dental

DTE

FDA UDI
Guilin Woodpecker Medical Instrument Co., Ltd.·06944843657769·Dental X-Ray Device

PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS

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

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

FDA 510(k)
FDA Class 1 ·General Hospital

BD VACUTAINER® K2 EDTA (K2E) PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 29, 2022

HAHN TAPERED IMPLANT 3.5 X 13MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 9, 2023

UNKNOWN LIGASURE INSTRUMENT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·December 17, 2021

HAHN TAPERED IMPLANT Ø3.5 X 13 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 24, 2024

HAHN TAPERED IMPLANT Ø3.5 X 13 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·August 6, 2024

HAHN TAPERED IMPLANT Ø3.5 X 13 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·March 28, 2024

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 21, 2013

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 26, 2014

VENTED AUTOFEED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·June 13, 2011