510(k) Report

FDA applicant

Dr. Fresh, Inc.

Houston, TX2 decisions2012–20120 recalls

FDA records 2 decisions for Dr. Fresh, Inc. (Houston, TX) in 2012: 2 510(k) clearances. Most are in product codes EEG (Heat Source For Bleaching Teeth) and LFD (Saliva, Artificial). Its devices cite 2 predicates, 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 Dr. Fresh, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2012

2012: 2
2012high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Dr. Fresh, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Which product codes does it file in?

  • EEGHeat Source For Bleaching Teeth1decision
  • LFDSaliva, Artificial1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K111250Dry Mouth MouthwashDr. Fresh, Inc. · 20122cite it

What has FDA decided for it lately?

  • K111250Dry Mouth MouthwashDr. Fresh, Inc. · 2012
  • K110888Absolute White LightDr. Fresh, Inc. · 2012

All 2 as Dr. Fresh, Inc. →