510(k) Report

FDA applicant

Voroba Technologies Assoc.

Minnetonka, MN2 decisions1986–19860 recalls

FDA records 2 decisions for Voroba Technologies Assoc. (Minnetonka, MN) in 1986: 2 510(k) clearances. Most are in product codes KHL (Hearing Aid, Master) and ESD (Hearing Aid, Air-Conduction, 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

FIG. A — Illustration, ear, nose and throat panel, where it files most

How often FDA has decided Voroba Technologies Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Voroba Technologies Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Voroba Technologies Assoc. 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?

  • KHLHearing Aid, Master1decision
  • ESDHearing Aid, Air-Conduction, Prescription1decision

What has FDA decided for it lately?

  • K860171Voroba Programmable Auditory ComparatorVoroba Technologies Assoc. · 1986
  • K860170Voroba Technologies, Assoc. Quantum Hearing AidVoroba Technologies Assoc. · 1986

All 2 as Voroba Technologies Assoc. →