Tearlab Corp

FDA Filings

This page includes the latest FDA filings for Tearlab Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

USAOTHER OTC MarketTEARDUNS 155813749
FDA Registration(s)
Registration Number3007137761
FEI Number3007137761
NameTearLab Corporation
Owner & OperatorTearLab Corporation
Contact Address150 La Terraza Blvd. Suite 101
Escondido CA 92025 US
Official Correspondent
  • Michael S Berg
  • x-760-2243563-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address150 La Terraza Blvd., Suite 101
Escondido, CA 92025 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Device in the United States for Export Only

FDA Filings

Device
Company
DeviceDate
Tearlab Corporation
 TearLab Osmolarity Test Card 2025-09-05
Tearlab Corporation
 Osmolarity High Control Solution 2024-01-15
Tearlab Corporation
 Osmolarity Normal Control Solutions 2024-01-15
Tearlab Corporation
 ScoutPro Osmolarity System 2022-12-14
TearLab Corporation
TearLab Discovery System2018-10-16
TearLab Corporation
TearLab Discovery MMP-9 Test2018-10-16
TearLab Corporation
TearLab Osmolarity System2009-07-08
TearLab Corporation
TearLab Osmolarity System2009-07-08

Related Finance Registrations
NCAGE Code5LYG6TEARLAB CORPORATION
CAGE Code5LYG6TEARLAB CORPORATION
SEC0001299139TearLab Corp of DELAWARE
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.