The following data is part of a premarket notification filed by Kerr Corporation with the FDA for Optibond Se.
| Device ID | K100347 |
| 510k Number | K100347 |
| Device Name: | OPTIBOND SE |
| Classification | Agent, Tooth Bonding, Resin |
| Applicant | KERR CORPORATION 1717 WEST COLLINS AVENUE Orange, CA 92867 |
| Contact | Wendy Garman |
| Correspondent | Wendy Garman KERR CORPORATION 1717 WEST COLLINS AVENUE Orange, CA 92867 |
| Product Code | KLE |
| CFR Regulation Number | 872.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-02-12 |
| Decision Date | 2010-04-30 |
| Summary: | summary |