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