96 results · 22ms · Sources: EU EUDAMED, US FDA

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ARIATELE TELEMETRY TRANSMITTER (96281)

FDA 510(k)
FDA Class 2 ·Cardiovascular

Micro Finger and Spatula

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896103030·Micro Finger and Spatula Double Ended Right Han...

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515234499·Shepard Bipolar Fcps, str

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613052485·Cushing Bayonet Bipolar Forcep 7 1/2" (190.5mm)...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613069018·Cushing Bayonet Bipolar Forcep 7 1/2" (190.5mm)...

MAXIFLEX - SEMI FLEX SCOPE, 25 TO 65 CM

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

EXTENSION SET LIGHT-SAFE, MODEL BC565

FDA 510(k)
FDA Class 2 ·General Hospital

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 4, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 4, 2017

EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·January 3, 2017

EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·February 2, 2016

EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 27, 2016

FGE CATHETER, BILIARY, DIAGNOSTIC - BILIARY STENT - METAL

FDA Adverse Event
Injury ·COOK INC·Product code FGE·January 29, 2020

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 31, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 30, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 30, 2019

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

FLEXI-SEAL FECAL MANAGEMENT SYSTME KIT

FDA Adverse Event
Malfunction ·CONVATEC, INC.·Product code KNT·July 29, 2014