FDA applicant
Livetec GmbH
FDA records 3 decisions for Livetec GmbH (Loerrach, DE) from 2013 to 2015: 3 510(k) clearances. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). 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 Livetec GmbH’s devices, and how often a recall has named them.
FDA decisions per year
1in 2015
2013high 1 (2013) · low 0 (2016)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2013.
Planning a device like Livetec GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report