17 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CLEARFIL MAJESTY ESTHETIC PLT
FDA 510(k)
FDA Class 2
·Dental
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290114691154·Titanium Base Abutment Round, Int. Hex. NP L6mm...
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108697971·Guided Countersink Ø3.25mm
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·September 14, 2007
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197194495·Tebbet Breast Retractor
70x25m...
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·September 28, 2007
WAKO AUTOKIT C4
FDA 510(k)
FDA Class 2
·Immunology
L.A.M. IPM WOUND GEL
FDA 510(k)
FDA Unclassified
·Unknown
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 24, 2024
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·October 4, 2007
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·December 3, 2007
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·November 5, 2007
ARROW BALLOON WEDGE CATHETER (X2)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code DYG·March 17, 2013
ATLAS
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·April 18, 2011
DIMENSION CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGONSTICS INC.·Product code JJE·June 27, 2008
PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBH·October 20, 2025
CADD-Solis VIP ambulatory Infusion Pumps, Model 2110. Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·August 14, 2024