FDA applicant

Clearlab Pte, Ltd.

Grand Junction, CO4 decisions2001–20060 recalls

FDA records 4 decisions for Clearlab Pte, Ltd. (Grand Junction, CO) from 2001 to 2006: 4 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 8 predicates, 1 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 Clearlab Pte, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clearlab Pte, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Clearlab Pte, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Clearlab”

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

Clearlab SG Pte, Ltd. 2

Clearlab Pte, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Clearlab”