Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022315836

FEI Number

3022315836

Entity Name

Vivos Therapeutics INC.

City/State/Country

Murray, KY, US

Establishment Address

300 S 5th Street, Murray, KY 42071, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Vivos Therapeutics, Inc. (Owner Number: 10054340)

Owner / Operator Contact Address

300 S 5th Street, Murray, KY 42071, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DNA Vivos Versa Vivos PEx Vivos DNA Appliance Vivos Vida Vivos mmRNA Appliance Vivos mRNA Appliance V-Starter Kids Vivos Grow (VG) Vivos Guide System Vivos Way (VW) V-Starter PreTeen Vivos Vida Sleep Vivos EMA Now Vivos Vida V-Starter Kids; V-Starter PreTeen; Vivos Grow (VG); Vivos Guide System; Vivos Way (VW) Facialblocks

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2023-04-13
LQZ	Device, Jaw Repositioning	Dental	Class 2	872.5570	2023-04-13
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2023-02-24
ECN	Clamp, Wire, Orthodontic	Dental	Class 1	872.5410	2023-01-18
DZC	Wire, Orthodontic	Dental	Class 1	872.5410	2017-09-14
MQC	Mouthguard, Prescription	Unknown	Class U	N/A	2023-04-06
LQZ	Device, Jaw Repositioning	Dental	Class 2	872.5570	2021-08-19
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2021-08-19
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2017-09-14
KMY	Positioner, Tooth, Preformed	Dental	Class 1	872.5525	2017-03-09
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2023-04-06
LQZ	Device, Jaw Repositioning	Dental	Class 2	872.5570	2023-04-06
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2023-01-18
LWF	Dilator, Nasal	Ear, Nose, Throat	Class 1	874.3900	2023-04-13
DYJ	Retainer, Screw Expansion, Orthodontic	Dental	Class 1	872.5410	2018-03-23

Official Correspondent

Kimberley Griffith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vivos Therapeutics, 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
K122391	Medtronic Xomed, Inc.	MEDTRONIC XOMED, INC.	2013-01-10
K112640	Ormco Corp.	HYPERELASTIC WIRE	2011-11-16

Similar Registrations

Registration Number	Establishment Name	Location
3030914478	GELB PRACTICE	Dix Hills, NY, US
3017092365	APNOMED, INC.	Bellevue, WA, US
3039643908	EMA-SLEEP INC	Bastrop, TX, US
3007108578	TRUE FUNCTION LABORATORY INC	La Mesa, CA, US
3006786034	Innovative Health Technologies (NZ) Limited	Dunedin Otago, NZ

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022315836. Last updated year: 2026. Please use registration number 3022315836 when referencing this establishment in official correspondence.