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

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STRONG DENTAL HANDPIECES

FDA 510(k)
FDA Class 1 ·Dental

Marienfeld Superior

FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317300096·

Dornier MedTech

FDA UDI
Dornier MedTech GmbH·04049958001536·600 Micron Disposable ND YAG Nozzle Tip Laser L...

COOLEY COARCTATION CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921001920·COOLEY COARCTATION CLAMP STRAIGHT JAW STRAIGHT ...

COOLEY COARCTATION CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896010147·COOLEY COARCTATION CLAMP STRAIGHT JAW STRAIGHT ...

LEONE SPA

FDA UDI
LEONE SPA·08033707085966·BKT F1000 SL DAMON SUPER TORQUE 22 KIT

Tasso-M20

FDA UDI
Tasso Inc.·00860006434540·The Tasso-M20 is used to collect, store, and tr...

MOBILE LINER ØINT 28 MM Ø42 MM

FDA Adverse Event
Malfunction ·LIMACORPORATE S.P.A.·Product code LZO·December 29, 2021

E3 MICROPROB SERIES OF LASERS AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MODULAR RADIAL HEAD SZ. 20S WW

FDA Adverse Event
Injury ·ASCENSION ORTHOPEDICS·Product code KWI·May 7, 2018

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 25, 2023

VERCISE GENUS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·January 5, 2024

ACUITY

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code OJX·May 8, 2013

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·September 18, 2014

TERUMO CDI 540 CALIBRATOR

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·May 16, 2011

MEDTRONIC SURGICAL TISSUE VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·August 9, 2021

DW ARTHROSCOPY FLUID MANAGEMENT DEV

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRX·August 9, 2019

MAIN PUMP TUBING

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRX·August 9, 2019

MAIN PUMP TUBING

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRX·August 9, 2019