510(k) Report

FDA applicant

Sentage Corporation D/B/A/ Dental Services Group

Washington, DC1 decision2003–20030 recalls

FDA records 1 decision for Sentage Corporation D/B/A/ Dental Services Group (Washington, DC) in 2003: 1 510(k) clearance. All are in product code MQC (Mouthguard, Prescription). No recall is linked to its devices.

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

How often FDA has decided Sentage Corporation D/B/A/ Dental Services Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sentage Corporation D/B/A/ Dental Services Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sentage Corporation D/B/A/ Dental Services Group 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?

  • MQCMouthguard, Prescription1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K022627DSG Relaxer SplintSentage Corporation D/B/A/ Dental Services Group · 20031cites it

What has FDA decided for it lately?

  • K022627DSG Relaxer SplintSentage Corporation D/B/A/ Dental Services Group · 2003

The one decision as Sentage Corporation D/B/A/ Dental Services Group →