Interval 7500
by Temrex Corp.
Interval 7500 is a Class II device made by Temrex Corp., cleared under FDA 510(k) K821824 on 6 Jul 1982 and listed in FDA GUDID since 13 Feb 2020 (UDI-DI 00850015110337), active 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 | Number00850015110337 | Date13 Feb 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK821824 | Date6 Jul 1982 | StatusActive |
Official records
- AccessGUDID record 00850015110337
- FDA 510(k) database K821824
Across registries
- FDA 510(k) K821824 decided 6 Jul 1982 Active
- FDA GUDID UDI-DI 00850015110337 listed 13 Feb 2020 Listed
Timeline
- Cleared FDA 510(k) K821824
- Listed FDA GUDID 00850015110337
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Interval
- Generic name
- Zinc phosphate dental cement
- Model / reference
- 7500
- Primary DI / UDI-DI
- 00850015110337
- 510(k) Number
- FDA product code
- EMA
- GMDN term
- Zinc phosphate dental cement
- Device class
- Class II
- Regulation number
- 872.3275
- GUDID distribution status
- In Commercial Distribution
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