510(k) Report

FDA applicant

Active Vertical Correctors, Inc.

Fort Wayne, IN2 decisions1984–19850 recalls

FDA records 2 decisions for Active Vertical Correctors, Inc. (Fort Wayne, IN) from 1984 to 1985: 2 510(k) clearances. All are in product code ECO (Spring, Orthodontic). 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 Active Vertical Correctors, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Active Vertical Correctors, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Active Vertical Correctors, Inc. 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?

  • ECOSpring, Orthodontic2decisions

What has FDA decided for it lately?

  • K844234Active Vertical Corrector ApplianceActive Vertical Correctors, Inc. · 1985
  • K843344Active Vertical Corrector Active BiteActive Vertical Correctors, Inc. · 1984

All 2 as Active Vertical Correctors, Inc. →

Other applicant names beginning “Active”

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

Active Electronics, Inc. 7Active Life Scientific, Inc. 3Active Corp. 1Active Optical Systems, Ltd. 1Active Signal Technologies, Inc. 1Active Protective Technologies, Inc. 1Active Optical Systems, Ltd./Efraim Bidas 1