10 results
·
36ms
·
Sources: EU EUDAMED, US FDA
LATTICE, INC.
FDA registration
LATTICE, INC.·2 products·🇺🇸 United States
NONE
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·February 26, 2026
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·July 30, 2025
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·May 21, 2026
LASIK SURGERY / EXCIMER LASER SYSTEM
FDA Adverse Event
Injury
·UNK·Product code LZS·June 7, 2018
AFFERA
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code QZI·November 21, 2025
AFFERA
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code QZI·August 8, 2025
LASER PROBES
FDA Adverse Event
Injury
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQE·March 13, 2019
LASER PROBES
FDA Adverse Event
Injury
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQE·March 13, 2019
Dimension Vista System CHEM 1 CAL, Catalog Number KC110, Lot Number 9DM001 The Dimension Vista CHEM 1 CAL is an in vitro diagnostic product for the calibration of Calcium (CA), Cholesterol (CHOL), Creatinine (CREA), Glucose (GLU), Lactic Acid (LA), Magnesium (MG), Thyroxine (T4), Thyronine Uptake (TU), Blood Urea Nitrogen (BUN) and Uric Acid (URCA) methods on the Dimension Vista System
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code JIX·August 31, 2009