510(k) Report

FDA applicant

Rolor Electronics Corp.

Hsin-Chu City, TW4 decisions2002–20020 recalls

FDA records 4 decisions for Rolor Electronics Corp. (Hsin-Chu City, TW) in 2002: 4 510(k) clearances. Most are in product codes ILY (Lamp, Infrared, Therapeutic Heating) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, physical medicine panel, where it files most

How often FDA has decided Rolor Electronics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rolor Electronics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Rolor Electronics Corp.’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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