The following data is part of a premarket notification filed by American Orthodontics with the FDA for Orthodontic Bite.
| Device ID | K922984 |
| 510k Number | K922984 |
| Device Name: | ORTHODONTIC BITE |
| Classification | Device, Anti-snoring |
| Applicant | AMERICAN ORTHODONTICS 1714 CAMBRIDGE AVE. Sheboygan, WI 53081 |
| Contact | Paul Riddle |
| Correspondent | Paul Riddle AMERICAN ORTHODONTICS 1714 CAMBRIDGE AVE. Sheboygan, WI 53081 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-22 |
| Decision Date | 1993-03-31 |