FDA applicant
G.I.E.- Gesellschaft Fur Lichttechnische Erzeugnisse Mbh
FDA records 1 decision for G.I.E.- Gesellschaft Fur Lichttechnische Erzeugnisse Mbh (Berlin, DE) in 2015: 1 510(k) clearance. All are in product code LEJ (Booth, Sun Tan). Its devices cite 1 predicate, 0 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
How often FDA has decided G.I.E.- Gesellschaft Fur Lichttechnische Erzeugnisse Mbh’s devices, and how often a recall has named them.
FDA decisions per year
1in 2015
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2015.
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