10,000 results · 178ms · Sources: EU EUDAMED, US FDA

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UNK - SCREWS: MATRIXMIDFACE

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code HWC·August 20, 2021

UNK - PLATES: MATRIXMIDFACE

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code JEY·August 20, 2021

H. PYLORI STAT - PAK

FDA Adverse Event
Other ·CHEMBIO DIAGNOSTIC SYSTEMS, INC.·Product code OWF·December 7, 2004

DERMABOND HV 0.5ML VIAL - 12EA

FDA Adverse Event
Injury ·ETHICON INC.·Product code MPN·November 12, 2025

VENTANA anti-Helicobacter Pylori (SP48) PAB 250, Catalog Number 06425623001, model 790-1015 Immunohistochemistry (IHC) for in vitro diagnostic use.

FDA Recall
Terminated ·Ventana Medical Systems Inc·Product code OWF·August 2, 2018

H. pylori (polyclonal} 1.0 mL Catalog number 215A-76; Hematology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

FDA Recall
Terminated ·Cell Marque Corporation·Product code OWF·May 5, 2017

Immunohistochemical Assay, Helicobacter Pylori

FDA classification
FDA Class 1 ·Immunohistochemical Assay, Helicobacter Pylori

OWL DENTAL

FDA registration
OWL DENTAL·5 products·🇺🇸 United States

OWO IMAGING LLC

FDA registration
OWO IMAGING LLC·1 product·🇺🇸 United States

DR.'S OWN, LLC

FDA registration
DR.'S OWN, LLC·1 product·🇺🇸 United States

TempShield

FDA UDI
Aion Biosystems, Inc.·00197644811199·The TempShield is a wearable device that senses...

ODFS PACE

FDA 510(k)
FDA Class 2 ·Neurology

ODFS Pace XL

FDA 510(k)
FDA Class 2 ·Neurology

WANG

FDA UDI
Conmed Corporation·20653405052736·WANG TRANSBRONCHIAL HISTOLOGY NEEDLE FOR PERIPH...

Subdural Electrode

FDA UDI
Ad-Tech Medical Instrument Corporation·00841823107114·

BWF-5 MEDICAL LASER SERIES

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

THE ODFS DROPPED FOOT STIMULATOR

FDA 510(k)
FDA Class 2 ·Neurology

BWF-5 MEDICAL LASER SERIES

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

OBF MODEL 112 VACUUM CUP SYSTEM

FDA 510(k)
FDA Class 2 ·Ophthalmic

OBF MODEL 115 COMPUTER TONOMETER SYSTEM

FDA 510(k)
FDA Class 2 ·Ophthalmic