FDA applicant

Venis DI A. Vendrame

Treviso, Italy, IT1 decision1993–19930 recalls

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

FDA decisions per year

No FDA decision for Venis DI A. Vendrame since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Venis”

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

Venis DI Alessandro Vendrame 1

Venis DI A. Vendrame

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Venis”