FDA applicant

Lakong Medical Device Company, Ltd.

City Of Industry, CA1 decision2011–20110 recalls

FDA records 1 decision for Lakong Medical Device Company, Ltd. (City Of Industry, CA) in 2011: 1 510(k) clearance. All are in product code ELC (Scaler, Ultrasonic). 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, dental panel, where it files most

How often FDA has decided Lakong Medical Device Company, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Lakong Medical Device Company, Ltd. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Lakong”

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

Lakong Medical Devices Co., Ltd. 2

Lakong Medical Device Company, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lakong”