# Kbl GmbH

- Location (FDA's records): Dernbach, DE
- FDA decisions: 2 (2016–2019): 2 510(k) clearances
- Names in FDA's records: Kbl GmbH (1); Kbl AG (1)
- Product codes: LEJ (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K151962: KBL Sunlamp Products (= Device Bundling name) (2016), cited by 1

## Recent decisions
- K191881: KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun (Oct 28, 2019)
- K151962: KBL Sunlamp Products (= Device Bundling name) (Sep 15, 2016)

Source page: https://510kreport.com/company/kbl