FDA UDI In Commercial Distribution 🇺🇸 United States

OASYS (Oral/Nasal Airway System)

DI: 00810002220210 · Model: 3014680794 · JOHN'S DENTAL LABORATORY INC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OASYS (Oral/Nasal Airway System)
Primary DI
00810002220210
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
1
Public Version Date
2023-04-05
Public Version Status
New
Public Device Record Key
8a54de22-d782-4546-bbe4-9dd82df6a7a9

Device Description

A removable intraoral device intended to reduce or alleviate snoring and obstructive sleep apnea in adults. This is a reusable device.

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
LWF Dilator, Nasal
LRK Device, Anti-Snoring

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00810002220210