Snore Bandit
Device, Anti-snoring
SnoreBandit LLC
The following data is part of a premarket notification filed by Snorebandit Llc with the FDA for Snore Bandit.
Pre-market Notification Details
| Device ID | K210910 |
| 510k Number | K210910 |
| Device Name: | Snore Bandit |
| Classification | Device, Anti-snoring |
| Applicant | SnoreBandit LLC 8176 Merlewood Ave Las Vegas, NV 89117 |
| Contact | Garry Thynne |
| Correspondent | Colette Cozean The EyeDeas Company 21581 Midcrest Dr. Lake Forest, CA 92630 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-03-29 |
| Decision Date | 2021-07-01 |
Trademark Results [Snore Bandit]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SNORE BANDIT 87140023 5282624 Live/Registered |
Thynne, Garry 2016-08-16 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.