Burbank Dental Laboratory

FDA Device Registration & Listing · Burbank, CA, US · Registration 3007233968

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
3007233968
FEI Number
3007233968
Entity Name
Burbank Dental Laboratory
City/State/Country
Burbank, CA, US
Establishment Address
2101 Floyd St, Burbank, CA 91504, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Burbank Dental Lab (Owner Number: 10043629)
Owner / Operator Contact Address
2101 Floyd St., Burbank, CA 91504, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Smart One Terrats Abutment BDL AB AB Dental Abutment Terrats Abutment Terrats Abutment BDL Keystone Keystone Abutment Tap III

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 2016-12-31
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2021-04-12
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2023-03-27
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2021-04-12
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2021-04-12
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2023-03-27
LRK Device, Anti-Snoring Dental Class 2 872.5570 2015-03-05

Official Correspondent

Revekka Geykher

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Burbank Dental Lab
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
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

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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3011587077 JIANGSU TRAUSIM MEDICAL INSTRUMENT CO.,LTD. Changzhou Jiangsu, CN
3012121192 DENTAL EVOLUTIONS, INC Beverly Hills, CA, US
3031529635 TRATE UAB Kaunas Kauno Apskritis, LT
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007233968. Last updated year: 2026. Please use registration number 3007233968 when referencing this establishment in official correspondence.
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