510(k) Report

FDA applicant

Light Tree Ventures Europe B.V.

Hague, NL13 decisions2022–20260 recalls

FDA records 13 decisions for Light Tree Ventures Europe B.V. (Hague, NL) from 2022 to 2026: 13 510(k) clearances. Most are in product codes OHS (Light Based Over The Counter Wrinkle Reduction) and OAP (Laser, Comb, Hair). Since 2016 its 510(k)s took a median of 109 days from receipt to decision, against 101 for FDA’s reviews in the same codes and years. Its devices cite 18 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, general and plastic surgery panel, where it files most

How often FDA has decided Light Tree Ventures Europe B.V.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2022: 42023: 72025: 12026 (partial year): 1
2022high 7 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Light Tree Ventures Europe B.V. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Light Tree Ventures Europe B.V.’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 “Light”

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