FDA applicant
Geske Beauty Tech GmbH
FDA records 1 decision for Geske Beauty Tech GmbH (Berlin, DE) in 2025: 1 510(k) clearance. All are in product code NFO (Stimulator, Transcutaneous Electrical…). Its devices cite 3 predicates, 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 Geske Beauty Tech GmbH’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2025high 1 (2025)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2025.
Planning a device like Geske Beauty Tech GmbH’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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