Siroendo
510(k) K052515
Siroendo is a Class I device made by SIRONA Dental Systems GmbH, cleared under FDA 510(k) K052515 on 31 Mar 2006, 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 | NumberK052515 | Date31 Mar 2006 | StatusActive |
Official records
- FDA 510(k) database K052515
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EKX
- Device class
- Class I
- Regulation
- 21 CFR Part 872.4200
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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