JOHNS DENTAL LABORATORY

FDA Device Registration & Listing · Terre Haute, IN, US · Registration 3014680794

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
3014680794
FEI Number
3014680794
Entity Name
JOHNS DENTAL LABORATORY
City/State/Country
Terre Haute, IN, US
Establishment Address
423 S 13th Street, Terre Haute, IN 47807, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Johns Dental Lab (Owner Number: 10058109)
Owner / Operator Contact Address
423 S 13th Street, Terre Haute, IN 47807, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Indirect Bonding Tray Vivos mRNA Elastic Mandibular Advancement (EMA) appliance Redline Redline Clear Aligner System Vivos DNA Vivos mmRNA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QJJ Indirect Bonding Tray Dental Class 1 872.5410 2024-11-07
LRK Device, Anti-Snoring Dental Class 2 872.5570 2018-08-26
LRK Device, Anti-Snoring Dental Class 2 872.5570 2024-11-07
NXC Aligner, Sequential Dental Class 2 872.5470 2022-06-14
LRK Device, Anti-Snoring Dental Class 2 872.5570 2023-03-09
LQZ Device, Jaw Repositioning Dental Class 2 872.5570 2023-03-09
LRK Device, Anti-Snoring Dental Class 2 872.5570 2022-01-18
LQZ Device, Jaw Repositioning Dental Class 2 872.5570 2022-01-18

Official Correspondent

Dawn Atkinson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Johns 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
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014680794. Last updated year: 2026. Please use registration number 3014680794 when referencing this establishment in official correspondence.
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