23 results · 29ms · Sources: EU EUDAMED, US FDA

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ALL SILICONE HEMATURIA CATHETER, MODELS 4861, 4862, 4863, 4864, 4865

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·10304040091637·FILE - Channels RF File - Size 25.06 29MM

Safco FG Diamonds

FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310211443·FG Diamond 813-020 amalgam remover regular 5/pack

ULTRAPOWER

FDA UDI
Conmed Corporation·10845854005576·ULTRAPOWER BUR, WIRE PASS (COPPER), 2MM

AUDIO TECHNOLOGIES S:R.1

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

AQUARIUS WORKSTATION

FDA 510(k)
FDA Class 2 ·Radiology

MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

FDA Adverse Event
Death ·ABBOTT MEDICAL·Product code NKM·November 18, 2024

MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code NKM·November 18, 2024

ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·June 16, 1997

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·March 26, 2013

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011

ICY HOT HEAT THERAPY PATCH

FDA Adverse Event
Other ·CHATTEM, INC.·Product code IMD·March 27, 2008

ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 31, 1997

ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·January 7, 1998

ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 23, 1997

ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 23, 1997

ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·August 12, 1997

ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, INC.·Product code GAG·October 9, 1997

1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015

Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system for clinical chemistry analysis.

FDA Enforcement
Class II ·Terminated·Roche Diagnostics Operations, Inc.·December 12, 2012