The following data is part of a premarket notification filed by James P Boyd with the FDA for Snorenti.
| Device ID | K032410 |
| 510k Number | K032410 |
| Device Name: | SNORENTI |
| Classification | Device, Jaw Repositioning |
| Applicant | JAMES P BOYD 710 MIDORI CT Solana Beach, CA 92075 |
| Contact | James P Boyd |
| Correspondent | James P Boyd JAMES P BOYD 710 MIDORI CT Solana Beach, CA 92075 |
| Product Code | LQZ |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-08-04 |
| Decision Date | 2005-02-28 |