FDA applicant

Tinnitus Treatment Centers, Inc.

Dallas, TX2 decisions1999–19990 recalls

FDA records 2 decisions for Tinnitus Treatment Centers, Inc. (Dallas, TX) in 1999: 2 510(k) clearances. All are in product code KLW (Masker, Tinnitus). Its devices cite 9 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 Treatment Centers, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tinnitus Treatment Centers, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Tinnitus Treatment Centers, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Tinnitus”

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

Tinnitus Control, Inc. 2 Tinnitus Otosound Products, LLC 1

Tinnitus Treatment Centers, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Tinnitus”