24 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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