EXPRESS DENTAL LABORATORY

FDA Device Registration & Listing · Moore, OK, US · Registration 3014093092

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
3014093092
FEI Number
3014093092
Entity Name
EXPRESS DENTAL LABORATORY
City/State/Country
Moore, OK, US
Establishment Address
300 N. Telephone Rd., Moore, OK 73160, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Express Dental Laboratory (Owner Number: 10088155)
Owner / Operator Contact Address
300 N. Telephone Rd., Moore, OK 73160, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Abutment, Implant. Dental, Endosseous - Preat Abutments Abutment, Implant, Dental, Endosseous-Preat Abutments

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2023-06-02
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2023-06-02

Official Correspondent

James Kirk

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Express Dental Laboratory
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
K211871 Faico Medical, LLC FAICO Dental Implant System and CAD/CAM Abutments 2021-11-18

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0007-2018 Implant Direct Sybron Manufacturing, LLC 2
Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014093092. Last updated year: 2026. Please use registration number 3014093092 when referencing this establishment in official correspondence.
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