Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029528165

FEI Number

3029528165

Entity Name

ACNIS TITANIUM & ALLOYS INC.

City/State/Country

Elk Grove Village, IL, US

Establishment Address

1940 E Devon Avenue, Elk Grove Village, IL 60007, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Acnis Titanium & Alloys Inc. (Owner Number: 10088899)

Owner / Operator Contact Address

1940 E Devon Avenue, Elk Grove Village, IL 60007, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NICRALLIUM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EJH	Alloy, Metal, Base	Dental	Class 2	872.3710	2026-05-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Acnis Titanium & Alloys Inc.

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029528165. Last updated year: 2026. Please use registration number 3029528165 when referencing this establishment in official correspondence.