Microlux/Blu
by Addent, Inc.
510(k) K072309
Microlux/Blu is a Class I device made by Addent, Inc., cleared under FDA 510(k) K072309 on 19 Nov 2007, 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 | FDA 510(k)SESE | NumberK072309 | Date19 Nov 2007 | StatusActive |
Official records
- FDA 510(k) database K072309
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EAZ
- Device class
- Class I
- Regulation
- 21 CFR Part 872.4630
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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