FDA applicant

Lutronic Vision, Inc.

Billerica, MA1 decision2022–20220 recalls

FDA records 1 decision for Lutronic Vision, Inc. (Billerica, MA) in 2022: 1 510(k) clearance. All are in product code HQF (Laser, Ophthalmic). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Lutronic Vision, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Lutronic Vision, Inc. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Lutronic”

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

Lutronic Corporation 29 Lutronic Global 1 Lutronic Aesthetic 1

Lutronic Vision, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Lutronic”