CO-ORAL-ITE DENTAL MFG. CO.

FDA Device Registration & Listing · DIAMOND SPRINGS, CA, US · Registration 2950685

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2950685
FEI Number
1000123591
Entity Name
CO-ORAL-ITE DENTAL MFG. CO.
City/State/Country
DIAMOND SPRINGS, CA, US
Establishment Address
6635 MERCHANDISE WAY, DIAMOND SPRINGS, CA 95619, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
CO-ORAL-ITE DENTAL MFG. CO. (Owner Number: 9005586)
Owner / Operator Contact Address
6635 MERCHANDISE WAY, --, Diamond Springs, CA 95619, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Teets

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2007-11-21

Official Correspondent

TYLER SUHOZA

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CO-ORAL-ITE DENTAL MFG. CO.
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
K800400 Dentsply Intl. MAXUM DENTURE RESIN 1980-03-12
K033020 Cmp Industries, LLC IMPAK ACRYLIC REPAIR RESIN LIQUID 2003-12-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2950685. Last updated year: 2026. Please use registration number 2950685 when referencing this establishment in official correspondence.
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