FDA UDI In Commercial Distribution 🇺🇸 United States

Vivos DNA

DI: 00810002220197 · Model: 3014680794 · JOHN'S DENTAL LABORATORY INC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vivos DNA
Primary DI
00810002220197
Version / Model
3014680794
Company Name
JOHN'S DENTAL LABORATORY INC
Labeler DUNS
016649253
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-13
Public Version
1
Public Version Date
2023-03-21
Public Version Status
New
Public Device Record Key
016adf6b-2358-487c-a2c2-cf5e519f7a8b

Device Description

Intraoral appliance intended to reduce snoring and/or mild to moderate obstructive sleep apnea (OSA) in adults over 18 years of age or older.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LRK Device, Anti-Snoring
LQZ Device, Jaw Repositioning

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00810002220197