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Data / Medical devices / United States / Aventix Medical Inc

Aventix Medical Inc: FDA-registered device maker in Laguna Hills, CA, United States, 1 510(k) clearance

Aventix Medical Inc is registered with the FDA (registration 3038675429) in Laguna Hills, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 27, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3038675429
Address
23282 Mill Creek Dr Ste 350, Laguna Hills, CA, United States, 92653
Owner or operator
Aventix Medical Inc (10095743)
Roles
Complaint file establishment, Repackager or relabeler, Specification developer
First device listed
April 22, 2026
Registered through
2026
Brand names listed
AVENTIX PFX System, NOVOCLEAR Device

Devices it lists

DeviceProduct codeClassRoleSource
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Complaint file establishment, Repackager or relabeler, 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
March 27, 2026K260255AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001)GEISubstantially EquivalentAventix Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated March 27, 2026. 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.