510(k) Report

FDA applicant

Jonathan A. Parker, D.D.S.

Washington, DC2 decisions1995–19960 recalls

FDA records 2 decisions for Jonathan A. Parker, D.D.S. (Washington, DC) from 1995 to 1996: 2 510(k) clearances. All are in product code LQZ (Device, Jaw Repositioning). 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 Jonathan A. Parker, D.D.S.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jonathan A. Parker, D.D.S. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jonathan A. Parker, D.D.S. 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?

  • LQZDevice, Jaw Repositioning2decisions

Who builds on its devices?

Later devices cite its devices 5 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.

  • K955503Adjustable PM PositionerJonathan A. Parker, D.D.S. · 19964cite it
  • K953293PM PositionerJonathan A. Parker, D.D.S. · 19951cites it

What has FDA decided for it lately?

  • K955503Adjustable PM PositionerJonathan A. Parker, D.D.S. · 1996
  • K953293PM PositionerJonathan A. Parker, D.D.S. · 1995

All 2 as Jonathan A. Parker, D.D.S. →