22 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TearScience, Inc.
FDA registration
TearScience, Inc.·4 products·🇺🇸 United States
MEIBOMIAN GLAND EVALUATOR
FDA UDI
TEARSCIENCE, INC.·00859623006018·MEIBOMIAN GLAND EVALUATOR - US
LIPIVIEW II OCULAR SURFACE INTERFEROMETE
FDA UDI
TEARSCIENCE, INC.·00859623006612·ASSEMBLY PKGD LIPIVIEW-2 - US
LIPIFLOW SYSTEM ACTIVATOR (DISPOSABLE)
FDA UDI
TEARSCIENCE, INC.·00859623006117·ACTIVATORS (BOX OF 10) US
LIPIFLOW SYSTEM ACTIVATOR II (DISPOSABLE
FDA UDI
TEARSCIENCE, INC.·00859623006315·ACTIVATORS (BOX OF 10) US
LIPIFLOW SYSTEM ACTIVATOR (DISPOSABLE)
FDA UDI
TEARSCIENCE, INC.·00859623006216·ACTIVATORS (BOX OF 10) US
LIPIFLOW SYSTEM ACTIVATOR II CABLE KIT
FDA UDI
TEARSCIENCE, INC.·00859623006711·KIT CABLE PKGD ACTIVATOR II - US
LIPIFLOW SYSTEM CONSOLE
FDA UDI
TEARSCIENCE, INC.·00859623006414·ASSEMBLY PKGD LIPIFLOW - US
MEIBOMIAN GLAND EVALUATOR
FDA UDI
TEARSCIENCE, INC.·00859623006919·ASSEMBLY PKGD LIPISCAN - US
MEIBOMIAN GLAND EVALUATOR
FDA UDI
TEARSCIENCE, INC.·00859623006001·MEIBOMIAN GLAND EVALUATOR - GBL,CH,AR
LIPIVIEW OCULAR SURFACE INTERFEROMETER
FDA UDI
TEARSCIENCE, INC.·00859623006513·ASSEMBLY PKGD LIPIVIEW 1 - INTL
LIPIFLOW SYSTEM ACTIVATOR II (DISPOSABLE)
FDA Adverse Event
Injury
·TEARSCIENCE, INC.·Product code ORZ·August 2, 2023
LIPIFLOW SYSTEM ACTIVATOR II (DISPOSABLE
FDA Adverse Event
Injury
·TEARSCIENCE, INC.·Product code ORZ·August 2, 2023
MEIBOMIAN GLAND EVALUATOR
FDA Adverse Event
Malfunction
·TEARSCIENCE, INC.·Product code HKI·July 9, 2025
LIPIFLOW
FDA Adverse Event
Injury
·TEARSCIENCE, INC.·Product code ORZ·July 13, 2018
LIPIFLOW THERMAL PULSATION SYSTEM
FDA Adverse Event
Injury
·TEARSCIENCE, INC.·Product code ORZ·August 2, 2017
LIPIFLOW
FDA Adverse Event
JOHNSON & JOHNSON/TEARSCIENCE, INC.·Product code ORZ·March 2, 2023
TEARSCIENCE LIPIFLOW THERMAL PULSATION SYSTEM
FDA Adverse Event
Injury
·JOHNSON & JOHNSON VISION / TEARSCIENCE, INC.·Product code ORZ·January 24, 2022
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation System is intended for use by physicians as a prescription device for the application of localized heat and pressure therapy in adult patients with chronic cystic conditions of the eyelids, including meibomian gland dysfunction (MGD), also known as evaporative dry eye or lipid deficiency dry eye.
FDA Recall
Terminated
·Tearscience, Inc·Product code ORZ·September 13, 2016
LipiFlow Thermal Pulsation System/LipiFlow, System Activator (Disposable), Rx Only, Sterile
FDA Recall
Terminated
·Tearscience, Inc·Product code ORZ·January 30, 2017