510(k) Report

FDA applicant

Selane Products, Inc.

Bradenton, FL2 decisions2013–20170 recalls

FDA records 2 decisions for Selane Products, Inc. (Bradenton, FL) from 2013 to 2017: 2 510(k) clearances. All are in product code LQZ (Device, Jaw Repositioning). Its devices cite 2 predicates, 1 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 Selane Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2013: 12017: 1
2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Selane Products, Inc. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Selane Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LQZDevice, Jaw Repositioning2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 6 times; 1 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.

  • K130130Atg/SM-Osa AppliancesSelane Products, Inc. · 20136cite it

What has FDA decided for it lately?

  • K162816SML-OSA2 AppliancesSelane Products, Inc. · 2017
  • K130130Atg/SM-Osa AppliancesSelane Products, Inc. · 2013

All 2 as Selane Products, Inc. →