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

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NATURELLE DAILY DISPOSABLE (HILAFILCON B) COSMETICALLY TINTED CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

Causse

FDA UDI
MEDTRONIC XOMED, INC.·00763000033361·PROSTHESIS 1112192 CAUSSE MUSHRM TOTAL

Causse

FDA UDI
MEDTRONIC XOMED, INC.·00681490033572·PROSTHESIS 1112192 CAUSSE MUSHRM TOTAL

n/a

FDA UDI
HANS RUDOLPH, INC.·00874750006175·4813 SERIES NON HTD PTM

INDISCAL DIGITAL MANOMETER

FDA 510(k)
FDA Class 2 ·General Hospital

DEFIBRILLATOR ANALYZER - DA-2006P

FDA 510(k)
FDA Class 2 ·Cardiovascular

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·April 1, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·April 1, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·July 2, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·PFIZER, INC.·Product code QJR·May 8, 2023

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 28, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 19, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·January 16, 2023

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 7, 2022

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015

STENT CORONARY

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code MAF·May 14, 2013

PARADIGM INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code LZG·September 23, 2014

OT ULTRALINK METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 3, 2011

INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FTR·January 2, 2024

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2022