FDA applicant

Clearlab SG Pte, Ltd.

Grand Junction, CO2 decisions2008–20190 recalls

FDA records 2 decisions for Clearlab SG Pte, Ltd. (Grand Junction, CO) from 2008 to 2019: 2 510(k) clearances. Most are in product codes MVN (Lens, Contact, (Disposable)) and LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 3 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 SG Pte, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Clearlab SG Pte, Ltd. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Other applicant names beginning “Clearlab”

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

Clearlab Pte, Ltd. 4

Clearlab SG 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”