FDA UDI In Commercial Distribution 🇺🇸 United States

O2Vent Mono (OVENT)

DI: 09351567000004 · Model: O2Vent Mono · OVENTUS MANUFACTURING PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
O2Vent Mono (OVENT)
Primary DI
09351567000004
Version / Model
O2Vent Mono
Company Name
OVENTUS MANUFACTURING PTY LTD
Labeler DUNS
748034696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-30
Public Version
1
Public Version Date
2019-06-07
Public Version Status
New
Public Device Record Key
1393c5db-a0e2-40d8-b08b-6ba705de6b17

Device Description

The OVENT device is for the treatment of snoring and/or obstructive sleep apnea and is comprised of: • A titanium bimaxillary oral appliance which comprises, in one device, a lower tray fitted over the lower teeth and an upper tray fitted over the upper teeth. • A dental polymer material in each tray which is in contact with and retaining in position, the user’s top and bottom teeth. • The lower jaw is retained in an advanced position to help open up the natural airway and alleviate the user’s snoring condition. • A breathing port at the front of the appliance with an enclosed airway on each side which passes between the teeth and the cheek. Each airway delivers the air at the rear of the mouth typically between the last teeth. The airways allow the user to breathe with the mouth closed.

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LRK Device, Anti-Snoring

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 09351567000004

Premarket Submissions

Submission Number Supplement Number
K160234 000