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Data / Medical devices / United States / Soberlink Healthcare LLC

Soberlink Healthcare LLC: FDA-registered device maker in Huntington Beach, CA, United States, 1 510(k) clearance

Soberlink Healthcare LLC is registered with the FDA (registration 3013019743) in Huntington Beach, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 14, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3013019743
Address
7711 Center Avenue #400, Huntington Beach, CA, United States, 92647
Owner or operator
Soberlink Healthcare LLC (10052354)
Roles
Complaint file establishment, Manufacturer, Specification developer
First device listed
July 19, 2016
Registered through
2026
Brand names listed
Soberlink Cellular Device and Sober Sky Web Portal

Devices it lists

DeviceProduct codeClassRoleSource
Devices, Breath Trapping, AlcoholDJZ1Complaint file establishment, Manufacturer, Specification developeraccessdata.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
July 14, 2016K160613Soberlink Cellular Device and Sober Sky Web PortalDJZSubstantially EquivalentSoberlink Healthcare, LLCaccessdata.fda.gov

Compare with other makers

Updated July 14, 2016. 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.