151 results · 18ms · Sources: EU EUDAMED, US FDA

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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