APOZA TOP Light
APOZA TOP Light is a Class II device made by Apoza Enterprise Co., Ltd., cleared under FDA 510(k) K041303 on 18 Jun 2004 and listed in FDA GUDID since 28 Jun 2023 (UDI-DI 04719883751478), 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 | Number04719883751478 | Date28 Jun 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK041303 | Date18 Jun 2004 | StatusActive |
Official records
- AccessGUDID record 04719883751478
- FDA 510(k) database K041303
Across registries
- FDA 510(k) K041303 decided 18 Jun 2004 Active
- FDA GUDID UDI-DI 04719883751478 listed 28 Jun 2023 Listed
Timeline
- Cleared FDA 510(k) K041303
- Listed FDA GUDID 04719883751478
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Apoza
- Generic name
- Dental/surgical polymerization lamp
- Model / reference
- TOP Light
- Primary DI / UDI-DI
- 04719883751478
- 510(k) Number
- FDA product code
- EBZ
- GMDN term
- Dental/surgical polymerization lamp
- Device class
- Class II
- Regulation number
- 872.6070
- GUDID distribution status
- In Commercial Distribution
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