FDA applicant
Linemaster Switch Corp.
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
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
Class I Class II/III not classified
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