510(k) Report

FDA applicant

Dale T. Dupuis

Opelousas, LA3 decisions1988–19880 recalls

FDA records 3 decisions for Dale T. Dupuis (Opelousas, LA) in 1988: 3 510(k) clearances. Most are in product codes EBL (Pin, Retentive And Splinting, And Accessory…) and EBF (Material, Tooth Shade, Resin). 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 Dale T. Dupuis’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dale T. Dupuis since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dale T. Dupuis by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Dale T. Dupuis’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?

  • EBLPin, Retentive And Splinting, And Accessory Instruments1decision
  • EBFMaterial, Tooth Shade, Resin1decision
  • EHOBar, Preformed1decision

What has FDA decided for it lately?

  • K883388Dentrek Bridge BarsDale T. Dupuis · 1988
  • K883074ElgiloyDale T. Dupuis · 1988
  • K882400Amorphus Silk by DentraxDale T. Dupuis · 1988

All 3 as Dale T. Dupuis →

Other applicant names beginning “Dale”

FDA records each applicant name separately; these may or may not be the same firm.

Dale Medical Products, Inc. 13Dale Miller, Inc. - the Chin-Up Company 1