FDA applicant

Glottal Ent., Inc.

Washington, DC1 decision1990–19900 recalls

FDA records 1 decision for Glottal Ent., Inc. (Washington, DC) in 1990: 1 510(k) clearance. All are in product code KLX (Electroglottograph). 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 Glottal Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Glottal Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Glottal Ent., Inc.

Which product codes does it file in?

What has FDA decided for it lately?