ORTHOCAD IQ
Bracket, Plastic, Orthodontic
CADENT, INC.
The following data is part of a premarket notification filed by Cadent, Inc. with the FDA for Orthocad Iq.
Pre-market Notification Details
| Device ID | K082207 |
| 510k Number | K082207 |
| Device Name: | ORTHOCAD IQ |
| Classification | Bracket, Plastic, Orthodontic |
| Applicant | CADENT, INC. 1700 PENNSYLVANIA AVE NW Washington, DC 20006 |
| Contact | Laurie Clarke |
| Correspondent | Laurie Clarke CADENT, INC. 1700 PENNSYLVANIA AVE NW Washington, DC 20006 |
| Product Code | DYW |
| Subsequent Product Code | EJF |
| Subsequent Product Code | NJM |
| CFR Regulation Number | 872.5470 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-05 |
| Decision Date | 2009-10-23 |
| Summary: | summary |
Trademark Results [ORTHOCAD IQ]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ORTHOCAD IQ 78842742 3490475 Dead/Cancelled |
ALIGN TECHNOLOGY, INC. 2006-03-21 |
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