FDA applicant

Tinnitus Control, Inc.

Washington, DC2 decisions2003–20060 recalls

FDA records 2 decisions for Tinnitus Control, Inc. (Washington, DC) from 2003 to 2006: 2 510(k) clearances. All are in product code KLW (Masker, Tinnitus). Its devices cite 3 predicates, 0 of them its own earlier devices. 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 Tinnitus Control, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tinnitus Control, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Tinnitus Control, 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

Other applicant names beginning “Tinnitus”

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

Tinnitus Treatment Centers, Inc. 2 Tinnitus Otosound Products, LLC 1

Tinnitus Control, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Tinnitus”