510(k) Report

FDA applicant

Linemaster Switch Corp.

Woodstock, CT1 decision2006–20062 recalls

FDA records 1 decision for Linemaster Switch Corp. (Woodstock, CT) in 2006: 1 510(k) clearance. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 5 predicates, 0 of them its own earlier devices. 2 recalls are 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 Linemaster Switch Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Linemaster Switch Corp. since 2007.

Recalls per year

1in 2010

2007: 12010: 1
2007high 1 (2007) · low 0 (2008)2026

Class I Class II/III not classified

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

Planning a device like Linemaster Switch 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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