Encore! MC-702
Encore! MC-702 is a Class II device made by Ortho Technology, Inc., cleared under FDA 510(k) K922499 on 30 Jul 1992 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00190730005007), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00190730005007 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK922499 | Date30 Jul 1992 | StatusActive |
Official records
- AccessGUDID record 00190730005007
- FDA 510(k) database K922499
Across registries
- FDA 510(k) K922499 decided 30 Jul 1992 Active
- FDA GUDID UDI-DI 00190730005007 listed 24 Sep 2016 Listed
Recalls
-
- Terminated Z-0876-2013
Orthodontic brackets distributed was incorrectly labeled.
Timeline
- Cleared FDA 510(k) K922499
- Recall initiated FDA recalls Z-0876-2013
- Listed FDA GUDID 00190730005007
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Encore!
- Generic name
- Orthodontic bracket, ceramic
- Model / reference
- MC-702
- Primary DI / UDI-DI
- 00190730005007
- 510(k) Number
- FDA product code
- NJM
- GMDN term
- Orthodontic bracket, ceramic
- Device class
- Class II
- Regulation number
- 872.5470
- GUDID distribution status
- In Commercial Distribution