Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018783058

FEI Number

3018783058

Entity Name

SCHLUMBOHM GMBH & CO. KG

City/State/Country

Brokstedt Schleswig-Holstein, DE

Establishment Address

Klein Floyen 8-10, Brokstedt Schleswig-Holstein 24616, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Schlumbohm GmbH & Co. KG (Owner Number: 10081593)

Owner / Operator Contact Address

Klein Floyen 8-10, Brokstedt, DE-SH 24616, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K202906

PMA Number

N/A

All Registered Proprietary Names

EndoPilot

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ELC	Scaler, Ultrasonic	Dental	Class 2	872.4850	2021-04-27
EKR	Plugger, Root Canal, Endodontic	Dental	Class 1	872.4565	2021-04-27
EKX	Handpiece, Direct Drive, Ac-Powered	Dental	Class 1	872.4200	2021-04-27
LQY	Locator, Root Apex	Unknown	Class U	N/A	2021-04-27

Official Correspondent

Gerald Schlumbohm

US Agent Details

Imke Lindenbeck Business: Komet USA LLC Email: ilindenbeck@komet-usa.com Phone: (888) 5663887

Related Public Records

Same Entity

Schlumbohm GmbH & Co. KG

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
K832443	California Technics, Inc.	ULTRASONIC DENTAL PROPHYLAXIS UNIT	1983-09-12
K994299	Bonart Co., Ltd.	ART-P3, MODEL P3-1-ART-A1	2000-03-06
K241065	Dentis Co., Ltd.	ChecQ (AC100)	2025-03-21

Similar Registrations

Registration Number	Establishment Name	Location
3042256012	QUANZHOU AGURU E-COMMERCE CO., LTD	Quanzhou Fujian, CN
1052939	Medidenta	Las Vegas, NV, US
3038718579	OKETZ LOGISTICS LLC	Coral Gables, FL, US
3003933619	MECTRON S.P.A.	CARASCO Genova, IT
9611253	NAKANISHI INC.	Kanuma Tochigi, JP

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018783058. Last updated year: 2026. Please use registration number 3018783058 when referencing this establishment in official correspondence.