Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006984721

FEI Number

3006984721

Entity Name

SCHOTT AG

City/State/Country

Mainz Rhineland-Palatinate, DE

Establishment Address

Otto Schott Strasse 2, Mainz Rhineland-Palatinate 55127, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SCHOTT AG (Owner Number: 10025267)

Owner / Operator Contact Address

Hattenbergstrasse 10, Mainz, DE-RP 55122, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Light, Fiberoptic, Dental Fiber Optic Rod

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EBZ	Activator, Ultraviolet, For Polymerization	Dental	Class 2	872.6070	2023-01-06

Official Correspondent

Joshua Beu

US Agent Details

Joshua Beu Business: SCHOTT North America Inc, - Lighting and Imaging Email: Joshua.beu@us.schott.com Phone: (508) 7653279

Related Public Records

Same Entity

SCHOTT AG

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
K243921	Foshan Coxo Medical Instrument Co., Ltd.	LED Curing Lights (DB686 HALO)	2025-04-11
K033201	Apoza Enterprise Co., Ltd.	LA500 BLUE LIGHT	2003-12-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006984721. Last updated year: 2026. Please use registration number 3006984721 when referencing this establishment in official correspondence.