FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
AlignerFlow LC
K Number: K231817
·
Decision Dec 1, 2023
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
119
Review Days
163
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Basic Information
- Device Name
- AlignerFlow LC
- K Number
- K231817
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3750
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Voco GmbH
- Date Received
- June 21, 2023
- Decision Date
- December 1, 2023
- Product Code
- DYH
- 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 |
|---|---|---|---|
| DYH | Adhesive, Bracket And Tooth Conditioner, Resin | FDA class 2 | Dental |
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