FDA applicant

Lasag AG

Eden Prairie, MN2 decisions1989–19900 recalls

FDA records 2 decisions for Lasag AG (Eden Prairie, MN) from 1989 to 1990: 2 510(k) clearances. Most are in product codes LXS (Laser, Neodymium:Yag, Ophthalmic For Posterior…) and HQF (Laser, Ophthalmic). 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 Lasag AG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lasag AG since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lasag”

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

Lasag Medical Lasers 2

Lasag AG

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lasag”