FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Solidex® Ti-Links and Screws
K Number: K251515
·
Decision Feb 10, 2026
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
1
Review Days
270
Basic Information
- Device Name
- Solidex® Ti-Links and Screws
- K Number
- K251515
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3630
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- CreoDent Hudson Valley
- Date Received
- May 16, 2025
- Decision Date
- February 10, 2026
- Product Code
- NHA
- 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 |
|---|---|---|---|
| NHA | Abutment, Implant, Dental, Endosseous | FDA class 2 | Dental |
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