FDA applicant

Venis DI Alessandro Vendrame

Treviso, Italy, IT1 decision1993–19930 recalls

FDA records 1 decision for Venis DI Alessandro Vendrame (Treviso, Italy, IT) in 1993: 1 510(k) clearance. All are in product code HQZ (Frame, Spectacle). 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 Venis DI Alessandro Vendrame’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Venis DI Alessandro Vendrame since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Venis DI Alessandro Vendrame’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

Other applicant names beginning “Venis”

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

Venis DI A. Vendrame 1

Venis DI Alessandro Vendrame

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Venis”