The following data is part of a premarket notification filed by Shofu Dental Corp. with the FDA for Beautibond Multi.
| Device ID | K110235 |
| 510k Number | K110235 |
| Device Name: | BEAUTIBOND MULTI |
| Classification | Agent, Tooth Bonding, Resin |
| Applicant | SHOFU DENTAL CORP. 1225 STONE DR. San Marcos, CA 92078 |
| Contact | David P Morais |
| Correspondent | David P Morais SHOFU DENTAL CORP. 1225 STONE DR. San Marcos, CA 92078 |
| Product Code | KLE |
| CFR Regulation Number | 872.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-01-26 |
| Decision Date | 2011-05-13 |