24 results · 20ms · Sources: EU EUDAMED, US FDA

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WEISS RETINAL CANNULA

FDA 510(k)
FDA Class 1 ·Ophthalmic

Endo Carry-on Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964150074·Endo Carry-on Procedure Kit Includes Basin, Def...

Axcent Acrylics

FDA UDI
GARRECO, LLC·D79330103050·DNT BASE REPR DK FIBER SC 5 LBS

GLACIER

FDA UDI
SDI LIMITED·DO3670103051·

Oxygen Sensor

FDA UDI
MERCURY ENTERPRISES, INC.·10641043103050·

Ovation Tribute Hip Stem

FDA UDI
Ortho Development Corporation·00822409010981·STD SIZE 5 Stem Plasma Spray

9616240-2006-00344

FDA Adverse Event
Malfunction ·Product code KDI·June 14, 2006

9616240-2006-00342

FDA Adverse Event
Malfunction ·Product code KDI·June 14, 2006

9616240-2006-00330

FDA Adverse Event
Malfunction ·Product code FII·June 1, 2006

MAC-LAB SYSTEM AND CARDIOLAB EP SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

HARDYDISK, CEFOXITIN, 30MCG

FDA 510(k)
FDA Class 2 ·Microbiology

9616240-2006-00349

FDA Adverse Event
Malfunction ·Product code FII·June 21, 2006

9616240-2006-00348

FDA Adverse Event
Malfunction ·Product code FDI·June 20, 2006

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FDA Adverse Event
Malfunction ·Product code FII·June 1, 2006

BD VACUTAINER® LH 68 I.U. PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 30, 2023

9616240-2006-00346

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007

JUVEDERM (VOLUME/CONCENTRATION UNKNOWN)

FDA Adverse Event
Injury ·ALLERGAN·Product code LMH·March 14, 2013

PYXIS ANESTHESIA SYSTEM (PAS)

FDA Adverse Event
Malfunction ·CAREFUSION·Product code BRY·February 11, 2011

Kendall MONOJECT MAGELLAN SAFETY NEEDLE 21G X 1 inch Product Number: 5551850110

FDA Recall
Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004