FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
SmarTooth
K Number: K231722
·
Decision May 1, 2024
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
23
Applicant Total
1
Review Days
323
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Basic Information
- Device Name
- SmarTooth
- K Number
- K231722
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.1745
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Smartooth Co., Ltd.
- Date Received
- June 13, 2023
- Decision Date
- May 1, 2024
- Product Code
- NBL
- 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 |
|---|---|---|---|
| NBL | Laser, Fluorescence Caries Detection | FDA class 2 | Dental |
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