32 results · 21ms · Sources: EU EUDAMED, US FDA

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MEDISIGN BLOOD GLUCOSE MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

NA

FDA UDI
Smith & Nephew, Inc.·03596010039019·HOKE OSTEOTOME 12.7MM X 127MM

JOBST Anti-Em

FDA UDI
BSN MEDICAL, INC.·00035664114565·ANTI EM TH M-LO W 6 EN FR ES

Kuglen Lens manipulator

FDA UDI
Medetz Surgical Instruments LLC·G2231114560·Kuglen Iris Hook And Lens Manipulator, Clover L...

Surgical Instrument

FDA UDI
Jeil Medical Corporation·08800089448852·

MicroSelectron Digital

FDA UDI
Nucletron B.V.·08717213032842·Coupling Treatment Tube for Metal Needles (16)

Custom Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964109157·Custom Procedure Kit

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964108310·Endo Carry-On Procedure Kit

Custom Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964109140·Custom Procedure Kit

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964108327·Endo Carry-On Procedure Kit

Custom Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964109676·Custom Procedure Kit

DELTA PLUS MULTIACTION SOLUTION FOR RIGID GAS PERMEABLE CONTACT LENSES

FDA 510(k)
FDA Class 2 ·Ophthalmic

ROCHE DIAGNOSTICS CALIBRATOR FOR AUTOMATED SYSTEMS, ROCHE DIAGNOSTICS CALIBRATOR CALIBRATOR FOR AUTOMATED SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 8, 2025

ASR UNI FEMORAL IMPL SIZE 45

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·May 14, 2013

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

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

ASR ACETABULAR CUPS 54

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 13, 2011

FLEXCATH ADVANCE STEERABLE SHEATH

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·November 13, 2019

ACHIEVE MAPPING CATHETER - 15 MM

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code DRF·November 13, 2019

RGDLOOP ADJUSTABLE STND

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SàRL·Product code MBI·April 6, 2020