9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PCA(R) MODULAR TOTAL KNEE TIB INSERT DUROCON BASEPLATE
FDA 510(k)
FDA Class 2
·Orthopedic
SOMNOTOUCH RESP
FDA 510(k)
FDA Class 2
·Anesthesiology
TSE-ANDERSON MODIFIED LACRIMAL GROOV
FDA 510(k)
FDA Class 1
·Ophthalmic
COVID ANTIGEN RAPID TEST KIT (SEALED SWAB IN BOX)
FDA Adverse Event
Injury
·IHEALTH LABS, INC.·Product code QKP·September 29, 2023
COVID ANTIGEN RAPID TEST KIT (SEALED SWAB IN BOX)
FDA Adverse Event
Injury
·IHEALTH LABS, INC.·Product code QKP·September 29, 2023
CLEARVIEW UTERINE MANIPULATOR
FDA Adverse Event
Injury
·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024
AKREOS ADVANCE ASPHERIC LENS
FDA Adverse Event
Injury
·BAUSCH & LOMB·Product code HQL·December 23, 2010
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 16, 2013
MINIMAX PLUS W/HARDSHELL
FDA Adverse Event
Injury
·PERFUSION SYSTEMS·Product code DTZ·July 17, 2014