151 results
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18ms
·
Sources: EU EUDAMED, US FDA
IMX ESTRADIOL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MAESTRO FOOT SWITCH
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023
MAESTRO 4000 POD, 100W
FDA Adverse Event
Malfunction
·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023
BLAZER II
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC DP TECHNOLOGIES·Product code LPB·October 10, 2007
Titan Modular Shoulder System 2.5
FDA UDI
Smith & Nephew, Inc.·00885556860069·CANNULATED CENTER STARTER DRILL
Titan Modular Shoulder System 2.5
FDA UDI
Smith & Nephew, Inc.·00885556860076·CANNULATED PEG DRILL
RUBICOR BREAST BIOPSY DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CORAL SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025
Titan™
FDA UDI
Ascension Orthopedics, Inc.·10381780244578·Titan™ Total Shoulder System
The cannulated peg...
Titan™
FDA UDI
Ascension Orthopedics, Inc.·10381780244561·Titan™ Total Shoulder System
The cannulated cen...
PINN MAR +4 10D 32IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 17, 2013
ENDEAVOR RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·December 3, 2010
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 8, 2014
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·EPT-1000 CARDIAC ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·MAESTRO 4000 CARDIAC ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI II COOLED ABLATION SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·BLAZER II TEMPERATURE ABLATION CATHETER, BLAZER II XP TEMPERATURE ABLATION CATHETER, BLAZER PRIME HTD TEMPERATURE ABLATI