510(k) Report

FDA applicant

Julie Alliance

Ormond Beach, FL2 decisions1999–20000 recalls

FDA records 2 decisions for Julie Alliance (Ormond Beach, FL) from 1999 to 2000: 2 510(k) clearances. Most are in product codes EIA (Unit, Operative Dental) and MUH (System, X-Ray, Extraoral Source, Digital). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Julie Alliance’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Julie Alliance since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Julie Alliance by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EIAUnit, Operative Dental1decision
  • MUHSystem, X-Ray, Extraoral Source, Digital1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K990002Quickray DSX 730Julie Alliance · 19992cite it

What has FDA decided for it lately?

  • K001445Smilie PCJulie Alliance · 2000
  • K990002Quickray DSX 730Julie Alliance · 1999

All 2 as Julie Alliance →

Other applicant names beginning “Julie”

FDA records each applicant name separately; these may or may not be the same firm.

Julie Williams, Pa-C 1