Data / Medical devices / United States / Allonrx LLC

Allonrx LLC: FDA-registered device maker in Lafayette, LA, United States, 1 510(k) clearance

Allonrx LLC is registered with the FDA (registration 3047516639) in Lafayette, LA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 25, 1996. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3047516639

Address

425 Settlers Trace Blvd Ste 202, Lafayette, LA, United States, 70508

Owner or operator

AllOnRx (10096049)

Roles

Complaint file establishment, Specification developer

First device listed

June 12, 2026

Registered through

2026

Brand names listed

Vortex

Devices it lists

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.

Compare with other makers

• All makers of Implant, Endosseous, Root-Form

Updated September 25, 1996. 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.