FDA applicant

Entravision, Inc.

Lenoir, NC3 decisions1986–19870 recalls

FDA records 3 decisions for Entravision, Inc. (Lenoir, NC) from 1986 to 1987: 3 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and HQE (Instrument, Vitreous Aspiration And Cutting…). 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, ophthalmic panel, where it files most

How often FDA has decided Entravision, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Entravision, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Entravision, 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

Entravision, Inc.

Which product codes does it file in?

What has FDA decided for it lately?