15 results
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19ms
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Sources: EU EUDAMED, US FDA
Clear Miracle
FDA 510(k)
FDA Class 2
·Dental
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221049742·Unitek(TM) Permachrome Standard Stainless Steel...
Nitinex Memory Staple
FDA UDI
VILEX LLC·00841731106810·Staple, Nitinex 25x16x16mm
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197448673·Micro Forceps
45° an...
MDT Diamond Coated Dental Burs
FDA UDI
M.D.T. - MICRO DIAMOND TECHNOLOGIES LTD.·07291046512128·Rotary FG gold diamond instrument for dental ap...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197392822·Micro Forceps
45° an...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197172714·Micro Forceps by Pierse
straig...
Puritan
FDA UDI
Puritan Medical Products·00609576381843·Sterile Foam Tipped Applicators
VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
FDA 510(k)
FDA Class 2
·Orthopedic
AT235
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
TERUMO SURGUARD2 SAFETY SYRINGE WITH NEEDLE
FDA Adverse Event
Malfunction
·TERUMO PHILIPPINES CORPORATION·Product code MEG·November 14, 2014
L9000 LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY - SAN JOSE·Product code FCW·August 30, 2011
ADVANTAGE SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 29, 2013
NAMIC Convenience Kit, LEFT HEART KIT, UPN H749600309351, REF/Catalog No. 60030935, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588. Product Usage: NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
FDA Enforcement
Class II
·Terminated·Navilyst Medical, Inc·March 4, 2015
Xper Flex Cardio Physiomonitoring System, Software versions 1.5.16.0322 and 1.6.1.0390, Model Numbers 453564241901, 453564241911, 453564483321, 453564483331, 453564621791, 453564621801, 453564669081
FDA Enforcement
Class II
·Terminated·Philips Electronics North America Corporation·December 26, 2018