33 results
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26ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Medline DeNovo 4Pro Electrical Stimulation Device
FDA 510(k)
FDA Class 2
·Physical Medicine
Pantheon System
FDA UDI
ADLER ORTHO SPA·08050880238514·Pantheon Bridging Collar Ø 36 mm for Stem Ø 20 mm
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958002625·Medilas HRM UroPulse Holmium Laser with wired f...
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003912·270 micron Holmium Laser Fiber Cable, Single Us...
AGXO
FDA UDI
Oticon A/S·05707131350299·G500 S, BTE PP 13 2.4G 105 C063 AGXO
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG
LIPOSUCTION CANNULA
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896009752·LIPOSUCTION CANNULA MERCEDES STYLE
LIPOSUCTION CANNULA
FDA UDI
SONTEC INSTRUMENTS, INC.·B0992012900·LIPOSUCTION CANNULA MERCEDES STYLE
Sklar®
FDA UDI
SKLAR CORPORATION·10649111347535·CRILE WOOD NH 9"
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197535915·GLASSMAN Gastro Intestinal Clamp,
280mm,...
BD SAFETY-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·December 3, 2024
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800113905207·VICEROY Rod - 6.0 (D)6x(L)290mm
Resorbable Mesh Pouch (Ballast MT, OsteoBallast MT)
FDA 510(k)
FDA Class 2
·Orthopedic
VISTA VISUALIZATION SYSTEM, MODEL 9000, VISTA VISUALIZATION SYSTEM WITH VOICE ACTIVATION AND PIP, MODEL 9100
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 1, 2023
OPTILITE® FREELITE® KAPPA FREE KIT
FDA Adverse Event
Injury
·THE BINDING SITE LIMITED·Product code DFH·March 30, 2026
OPTILITE® FREELITE® KAPPA FREE KIT
FDA Adverse Event
Injury
·THE BINDING SITE LIMITED·Product code DFH·March 31, 2026
VITEK® 2 GRAM POSITIVE ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LQL·August 29, 2018
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·August 3, 2011
AUTOPULSE® RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION·Product code DRM·October 27, 2014