FDA 510(k)
FDA class 2
Substantially Equivalent
🇪🇸 Spain
CeraRoot TL Implant System (TL)
K Number: K242072
·
Decision May 14, 2025
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
1
Review Days
302
Basic Information
- Device Name
- CeraRoot TL Implant System (TL)
- K Number
- K242072
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- CeraRoot SL
- Date Received
- July 16, 2024
- Decision Date
- May 14, 2025
- Product Code
- DZE
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | FDA class 2 | Dental |
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