FDA applicant

Glasspan, Inc.

Washington, DC1 decision1994–19940 recalls

FDA records 1 decision for Glasspan, Inc. (Washington, DC) in 1994: 1 510(k) clearance. All are in product code ELS (Splint, Endodontic Stabilizing). 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 Glasspan, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Glasspan, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Glasspan, 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

Glasspan, Inc.

Which product codes does it file in?

What has FDA decided for it lately?