510(k) Report

FDA applicant

Tuco Innovations, Inc.

Littleton, CO1 decision2002–20020 recalls

FDA records 1 decision for Tuco Innovations, Inc. (Littleton, CO) in 2002: 1 510(k) clearance. All are in product code NHN (Powered Light Based Laser Non-Thermal…). 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, physical medicine panel, where it files most

How often FDA has decided Tuco Innovations, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tuco Innovations, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Tuco Innovations, 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?

  • NHNPowered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive…1decision

Who builds on its devices?

Later devices cite its devices 5 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.

  • K012580Erchonia PL2000Tuco Innovations, Inc. · 20025cite it

What has FDA decided for it lately?

  • K012580Erchonia PL2000Tuco Innovations, Inc. · 2002

The one decision as Tuco Innovations, Inc. →