Corix 70 Corix 70 Plus USV
Corix 70 Corix 70 Plus USV is a Class II device made by Coramex, S.A., cleared under FDA 510(k) K031802 on 21 Jul 2003 and listed in FDA GUDID since 10 Jan 2024 (UDI-DI 00860010674406), active as of 22 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 | Number00860010674406 | Date10 Jan 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK031802 | Date21 Jul 2003 | StatusActive |
Official records
- AccessGUDID record 00860010674406
- FDA 510(k) database K031802
Across registries
- FDA 510(k) K031802 decided 21 Jul 2003 Active
- FDA GUDID UDI-DI 00860010674406 listed 10 Jan 2024 Listed
Timeline
- Cleared FDA 510(k) K031802
- Listed FDA GUDID 00860010674406
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Corix 70
- Generic name
- Stationary extraoral dental x-ray system, analogue
- Model / reference
- Corix 70 Plus USV
- Primary DI / UDI-DI
- 00860010674406
- 510(k) Number
- FDA product code
- EHD
- GMDN term
- Stationary extraoral dental x-ray system, analogue
- Device class
- Class II
- Regulation number
- 872.1800
- GUDID distribution status
- In Commercial Distribution
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