510(k) Report

FDA applicant

Advanced Technology Research (A.T.R.) S.R.P.

Lake Forest, CA2 decisions1999–20000 recalls

FDA records 2 decisions for Advanced Technology Research (A.T.R.) S.R.P. (Lake Forest, CA) from 1999 to 2000: 2 510(k) clearances. All are in product code EFB (Handpiece, Air-Powered, Dental). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Advanced Technology Research (A.T.R.) S.R.P.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Technology Research (A.T.R.) S.R.P. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Technology Research (A.T.R.) S.R.P. 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?

  • EFBHandpiece, Air-Powered, Dental2decisions

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 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.

  • K000547Atr TecnikaAdvanced Technology Research (A.T.R.) S.R.P. · 20002cite it
  • K991401Atr 3000, Atr 2000, Implant-ProAdvanced Technology Research (A.T.R.) S.R.P. · 19991cites it

What has FDA decided for it lately?

  • K000547Atr TecnikaAdvanced Technology Research (A.T.R.) S.R.P. · 2000
  • K991401Atr 3000, Atr 2000, Implant-ProAdvanced Technology Research (A.T.R.) S.R.P. · 1999

All 2 as Advanced Technology Research (A.T.R.) S.R.P. →