Tearscience, Inc. - FDA 510(k) Cleared Devices
9
Total
8
Cleared
1
Denied
Tearscience, Inc. has 8 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Historical record: 8 cleared submissions from 2009 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Tearscience, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Tearscience, Inc.
9 devices
Cleared
Oct 22, 2019
LipiFlow Thermal Pulsation System
Ophthalmic
29d
Cleared
Dec 10, 2018
LipiScan Dynamic Meibomian Imager
Ophthalmic
89d
Cleared
Nov 04, 2016
LipiFlow Thermal Pulsation System
Ophthalmic
172d
Cleared
Jan 14, 2016
LipiView II Ocular Surface Interferometer
Ophthalmic
106d
Cleared
Dec 23, 2013
LIPIFLOW THERMAL PULSATION SYSTEM
Ophthalmic
84d
Cleared
Dec 31, 2012
LIPIVIEW OCULAR SURFACE INTERFEROMETER
Ophthalmic
139d
Cleared
Dec 19, 2011
LIPIFLOW THERMAL PULSATION SYSTEM
Ophthalmic
94d
Not Cleared
Jun 28, 2011
LIPFLOW THERMAL PULSATION SYSTEM (FORMERLY MANUAL MINI SYSTEM)
Ophthalmic
323d
Cleared
Oct 23, 2009
LIPIVIEW OCULAR SURFACE INTERFEROMETER
Ophthalmic
115d