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Data / Medical devices / United States / Click Therapeutics, Inc.

Click Therapeutics, Inc.: FDA-registered device maker in New York, NY, United States, 1 510(k) clearance

Click Therapeutics, Inc. is registered with the FDA (registration 3031465632) in New York, NY, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 11, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3031465632
Address
80 White St 3rd Floor, New York, NY, United States, 10013
Owner or operator
Click Therapeutics, Inc. (10090983)
Roles
Complaint file establishment, Contract manufacturer, Manufacturer
First device listed
June 24, 2024
Registered through
2026
Brand names listed
CT-132

Devices it lists

DeviceProduct codeClassRoleSource
Computerized Behavioral Therapy Device For Depressive Disorders.SAP2Contract manufactureraccessdata.fda.gov
Computerized Behavioral Therapy Device For MigraineSEE2Complaint file establishment, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 11, 2025DEN240064CT-132SEEUnknownClick Therapeutics, Inc.accessdata.fda.gov

Compare with other makers

Updated April 11, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.