FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BracePaste Prime Plus
K Number: K261840
·
Decision Jun 3, 2026
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
45
Review Days
1
Basic Information
- Device Name
- BracePaste Prime Plus
- K Number
- K261840
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3750
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- American Orthodontics
- Date Received
- June 2, 2026
- Decision Date
- June 3, 2026
- Product Code
- DYH
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DYH | Adhesive, Bracket And Tooth Conditioner, Resin | FDA class 2 | Dental |
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