12 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STYLET, MODELS 4060, 4062, 4064, 4090, 4091 AND 4078
FDA 510(k)
FDA Class 2
·Cardiovascular
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036027438·
RTE SNAPCONE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FHW·July 11, 2023
PM 2002 PROLINE/AEC
FDA 510(k)
FDA Class 2
·Dental
ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925
FDA 510(k)
FDA Class 1
·Dental
INFINION 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 4, 2024
REAR TIP EXTENDER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code N/A·December 30, 2025
RTE SNAPCONE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FHW·February 17, 2021
UNKNOWN LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015
RIATA PASSIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 2, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·May 5, 2011
ARTICUL/EZE BALL 32 +5 BR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code JDI·July 30, 2008