FDA applicant

Lapis Lazuli International NV

Grand Junction,, CO1 decision2007–20070 recalls

FDA records 1 decision for Lapis Lazuli International NV (Grand Junction,, CO) in 2007: 1 510(k) clearance. All are in product code LPN (Accessories, Soft Lens Products). 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 Lapis Lazuli International NV’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lapis”

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

Lapis Lazuli, NV 1

Lapis Lazuli International NV

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Lapis”