Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020195105

FEI Number

3020195105

Entity Name

REALLOY E.K.

City/State/Country

Krefeld North Rhine-Westphalia, DE

Establishment Address

Moerser Strasse 232, Krefeld North Rhine-Westphalia 47803, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Realloy e.K. (Owner Number: 10082496)

Owner / Operator Contact Address

Moerser Strasse 232, Krefeld, DE-NW 47803, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Realloy BC Softblank Realloy BC Softblank R Realloy LFC Realloy CH Blank Realloy Classic Softblank Realloy C Blank Realloy Laserwire Realloy Classic Realloy N+ Realloy C Realloy C Softblank R Realloy C Powder Realloy Classic Softblank R Realloy Base Realloy C Softblank Realloy CH Realloy N Realloy BC Modell FH Realloy Ga280 Realloy Universal Solder Realloy BC Powder Realloy Classic Powder Realloy BC Blank Modell EH

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EJH	Alloy, Metal, Base	Dental	Class 2	872.3710	2021-08-04

Official Correspondent

Serdar Baysan

US Agent Details

German American Chamber of Commerce, Inc. German American Ch Email: legalservices@gaccny.com Phone: (212) 9748830

Related Public Records

Same Entity

Realloy e.K.

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
K810521	C.Vaupel Dental, Inc.	CO-SPAN 13.5 CASTING ALLOY	1981-03-17

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3010605319	Adentatec GmbH	Woerth am Main Bavaria, DE
3039443707	SHANGHAI FRONTIER MATERIAL TECH CO., LTD.	Shanghai, CN
2014676	The Belport Company, Inc DBA Gingi-Pak	CAMARILLO, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020195105. Last updated year: 2026. Please use registration number 3020195105 when referencing this establishment in official correspondence.