510(k) Report

FDA applicant

Hoya Lamphun, Ltd.

Amphur Muang, TH2 decisions2024–20260 recalls

FDA records 2 decisions for Hoya Lamphun, Ltd. (Amphur Muang, TH) from 2024 to 2026: 2 510(k) clearances. Most are in product codes LPL (Lenses, Soft Contact, Daily Wear) and MVN (Lens, Contact, (Disposable)). Its devices cite 3 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “HOYA Lamphun , Ltd.”.

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 Hoya Lamphun, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024: 12026 (partial year): 1
2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Hoya Lamphun, Ltd. by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hoya Lamphun, 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 “Hoya”

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