510(k) DEN100017

Device
LIPFLOW THERMAL PULSATION SYSTEM (FORMERLY MANUAL MINI SYSTEM)
Applicant
Tearscience, Inc.
510(k) number
DEN100017
Product code
ORZ
Decision
Unknown (DENG)
Decision date
2011-06-28
Date received
2010-08-09
Regulation
886.5200
Classification name
Eyelid Thermal Pulsation System
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Post-NSE
Third party reviewed
N

Applicant Contact#

Contact
CHRISTY MOENY
Address
1101 G Aviation Pkwy. Morrisville NC US 27560 27560

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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K240512Tixel i (TXLI0001)Novoxel , Ltd.2024-11-04
K231084TearCare MGX SystemSight Sciences, Inc.2023-12-27
K213045TearCare SystemSight Sciences, Inc.2021-12-21
K200400Systane iLux2Tear Film Innovations, Inc.2020-05-21
K192623LipiFlow Thermal Pulsation SystemTearscience, Inc.2019-10-22
K172645iLux Instrument, iLux DisposableTear Film Innovations, Inc.2017-12-26
K161357LipiFlow Thermal Pulsation SystemTearscience, Inc.2016-11-04
K133127LIPIFLOW THERMAL PULSATION SYSTEMTearscience, Inc.2013-12-23
K112704LIPIFLOW THERMAL PULSATION SYSTEMTearscience, Inc.2011-12-19