FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
els unibond
K Number: K252151
·
Decision Dec 5, 2025
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
4
Review Days
149
Basic Information
- Device Name
- els unibond
- K Number
- K252151
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3200
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Saremco Dental AG
- Date Received
- July 9, 2025
- Decision Date
- December 5, 2025
- Product Code
- KLE
- 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 |
|---|---|---|---|
| KLE | Agent, Tooth Bonding, Resin | FDA class 2 | Dental |
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