# KBL GmbH

FEI: 3006116732
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: KBL  GmbH (#10030591)

Address: Ringstrasse 24-26, Dernbach Rhineland-Palatinate, 56307, DE

Mandatory US Agent: Bentley Biomedical Consulting LLC

## Products

Total registered: 1
Top product codes: LEJ
Regulation §: 878.4635

Proprietary names: KBL 7000 alpha hybridSun, KBL 8000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL P9S hybridSun, KBL P9 hybridSun, KBL K5 hybridSun, KBL K7S hybridSun, KBL K7 hybridSun, KBL K9S hybridSun

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006116732%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006116732