Cleo 002-22-000010
by American Orthodontics 2 variants
Cleo 002-22-000010, an orthodontic bracket (FDA Class II; FDA product code NJM, Bracket, ceramic, orthodontic) made by American Orthodontics, was cleared under FDA 510(k) K232011 on 7 Jul 2023 and listed in FDA GUDID on 14 Jan 2025 (UDI-DI 00190746064425); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00190746064425 | Date14 Jan 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK232011 | Date7 Jul 2023 | StatusActive |
Official records
- AccessGUDID record 00190746064425
- FDA 510(k) database K232011
Across registries
- FDA 510(k) K232011 decided 7 Jul 2023 Active
- FDA GUDID UDI-DI 00190746064425 listed 14 Jan 2025 Listed
Timeline
- Cleared FDA 510(k) K232011
- Listed FDA GUDID 00190746064425
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cleo
- Generic name
- Orthodontic bracket, ceramic
- Model / Ref / Catalog
- 002-22-000010
- Primary DI / UDI-DI
- 00190746064425
- 510(k) Number
- FDA product code
- NJM
- GMDN term
- Orthodontic bracket, ceramic
- Device class
- Class II
- Regulation number
- 872.5470
- GUDID distribution status
- Not in Commercial Distribution
- MRI safety
- MR Safe
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