FDA applicant

Astralite Corp.

Van Nuys, CA2 decisions1989–20030 recalls

FDA records 2 decisions for Astralite Corp. (Van Nuys, CA) from 1989 to 2003: 2 510(k) clearances. Most are in product codes EOB (Nasopharyngoscope (Flexible Or Rigid)) and FSS (Light, Surgical, Floor Standing). 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 Astralite Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Astralite Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Astralite Corp.’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

Astralite Corp.

Which product codes does it file in?

What has FDA decided for it lately?