LRK · Class II · 21 CFR 872.5570

FDA Product Code LRK: Device, Anti-snoring

Oral appliance therapy provides an effective non-CPAP option for snoring and mild obstructive sleep apnea. FDA product code LRK covers anti-snoring devices worn in the mouth during sleep.

These mandibular advancement or tongue retention devices reposition the jaw or tongue to maintain airway patency during sleep, reducing snoring and apnea events. They are custom-fabricated or thermoplastic appliances worn during sleep.

LRK devices are Class II medical devices, regulated under 21 CFR 872.5570 and reviewed by the FDA Dental panel.

Leading manufacturers include Prismatik Dentalcraft, Inc., Good Sleep CO Pte , Ltd. and Fissiontech, LLC.

210
Total
210
Cleared
175d
Avg days
1988
Since
210 devices
49–72 of 210
No devices found for this product code.