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

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CHISON, MODEL 8300

FDA 510(k)
FDA Class 2 ·Radiology

Channel Drain

FDA UDI
C. R. Bard, Inc.·00801741049750·Channel Drain, 7mm Flat 3/4 Fluted

NIDO Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07315K0122100·T-Handle, Head Persuader

Genius Total Knee System

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215021641·

SYNTRA DIALYZER, MODEL SYNTRA 120, 160

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

MODIFICATION TO ACCU-CHEK INFORM METER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Crescendo Meniscal Insert CR Ultracongruent 12mm Size 0

FDA UDI
AMPLITUDE SAS·03701089524728·

CADD CASSETTE 100ML W/FLOWSTOP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·June 23, 2021

CADD MEDICATION CASSETTE

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·June 1, 2021

NUVASIVE

FDA Adverse Event
Injury ·NUVASIVE·Product code NKB·January 10, 2011

UNKNOWN

FDA Adverse Event
Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

UNK

FDA Adverse Event
Injury ·COOK, INC.·Product code DTK·August 20, 2014

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DTK·August 20, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 28, 2011

CAPSURE SP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008

GUNTHER TULIP VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·April 3, 2026

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·September 12, 2017

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·November 11, 2021

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·December 5, 2017