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Data / Medical devices / United States / Avant Wellness Systems Inc

Avant Wellness Systems Inc: FDA-registered device maker in Thousand Oaks, CA, United States, 1 510(k) clearance

Avant Wellness Systems Inc is registered with the FDA (registration 3010162243) in Thousand Oaks, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 3, 2013. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3010162243
Address
2706 Conejo Center Dr, Thousand Oaks, CA, United States, 91320
Owner or operator
Avant Wellness Systems (10048687)
Roles
Complaint file establishment, Manufacturer
First device listed
February 11, 2015
Registered through
2026
Brand names listed
LZ30-Home, LZ30-MaxIR, LZ30-MaxR, LZ30-P, LZ30-ProX, LZ30-ProZ, LZ30-Revi, LZ30-X and more

Devices it lists

DeviceProduct codeClassRoleSource
Lamp, Infrared, Therapeutic HeatingILY2Complaint 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
December 3, 2013K123474AVANT LASERILYSubstantially EquivalentAvant Wellness Systems, LLCaccessdata.fda.gov

Compare with other makers

Updated December 3, 2013. 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.