The following data is part of a premarket notification filed by Ormco Corp. with the FDA for Hyperelastic Wire.
| Device ID | K112640 |
| 510k Number | K112640 |
| Device Name: | HYPERELASTIC WIRE |
| Classification | Wire, Orthodontic |
| Applicant | ORMCO CORP. 1717 WEST COLLINS AVENUE Orange, CA 92867 |
| Contact | Wendy Garman |
| Correspondent | Wendy Garman ORMCO CORP. 1717 WEST COLLINS AVENUE Orange, CA 92867 |
| Product Code | DZC |
| CFR Regulation Number | 872.5410 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-09-12 |
| Decision Date | 2011-11-16 |
| Summary: | summary |