Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2027244

FEI Number

2027244

Entity Name

NEODONTICS INC

City/State/Country

Sun Valley, CA, US

Establishment Address

9775 Glenoaks Blvd, No. H, Sun Valley, CA 91352, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

NEODONTICS, INC. (Owner Number: 10027368)

Owner / Operator Contact Address

1266 Elm Avenue, Glendale, CA 91201, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NEOALLOY NEOTITAN ZAIRE CERAMIC ALLOYS w/o Be. NEOTITAN-PD NEOCAST S NEOCAST V NICROMED COBAFLEX-3 COBAFLEX-1 CERAMIC ALLOYS w/Be. FORMULA 45+Ti NEOCAST C P.D. ALLOYS (PARTIAL DENTURE ALLOYS) NEODONTICS, INC. -PRODUCT NAMES NICROLITE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EJH	Alloy, Metal, Base	Dental	Class 2	872.3710	2009-06-08

Official Correspondent

SAMUEL BABAYAN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NEODONTICS, 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 2027244. Last updated year: 2026. Please use registration number 2027244 when referencing this establishment in official correspondence.