FDA UDI In Commercial Distribution 🇺🇸 United States

The Luco Hybrid OSA Appliance

DI: 00810002220241 · Model: 3014680794 · JOHN'S DENTAL LABORATORY INC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
The Luco Hybrid OSA Appliance
Primary DI
00810002220241
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
2023-03-28
Public Version
2
Public Version Date
2023-12-25
Public Version Status
Update
Public Device Record Key
da13e98e-a445-46e6-86dd-17b193263aae

Device Description

An intraoral device designed to treat primary snoring and mild to moderate obstructive sleep apnea, as well as sleep bruxism and aid in the treatment of associated tension/migraine type headaches in adults. This device is reusable.

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
OCO Mouthguard, Migraine/Tension Headache
MQC Mouthguard, Prescription

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00810002220241