Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006116732

FEI Number

3006116732

Entity Name

KBL GmbH

City/State/Country

Dernbach Rhineland-Palatinate, DE

Establishment Address

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

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

KBL GmbH (Owner Number: 10030591)

Owner / Operator Contact Address

Ringstrasse 24-26, Dernbach, DE-RP 56307, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K151962

PMA Number

N/A

All Registered Proprietary Names

KBL A6 extraSun+ KBL A5 extraSun+ KBL Tower space 2000 KBL 7900 alpha KBL Tower space 3000 KBL 6800 alpha KBL 6700 alpha KBL 5600 alpha KBL 4800 alpha KBL Tower pure Energy 5 KBL 8000 alpha extraSun KBL 7000 alpha extraSun KBL P9 extraSun KBL P9S extraSun KBL 5600 alpha extraSun+ KBL 7000 alpha extraSun+ KBL 6800 alpha extraSun+ KBL 7900 alpha extraSun+ KBL 8000 alpha extraSun+ KBL Tower space 3000 hybridSun KBL 4800 alpha extraSun+ KBL K7 pureSun KBL Tower pure Energy 5 hybridSun KBL K5 pureSun KBL K5 extraSun KBL K11 Air (Loft) KBL K7S pureSun KBL K7S extraSun KBL K7 extraSun KBL K9S extraSun KBL K9S vitaSun

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LEJ	Booth, Sun Tan	General, Plastic Surgery	Class 2	878.4635	2016-11-11

Official Correspondent

Ralf de Andreis

US Agent Details

Shepard Bentley Business: Bentley Biomedical Consulting LLC Email: sbentley@bentleybiomed.com Phone: (949) 3749187

Related Public Records

Same Entity

KBL GmbH

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K875190	Ultra Tan Intl. AB	ULTRA TAN PURPLE PRO	1988-01-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006116732. Last updated year: 2026. Please use registration number 3006116732 when referencing this establishment in official correspondence.