K231817
- 510(k) number
- K231817
- Device name
- AlignerFlow LC
- Applicant
- Voco GmbH DE
- Product code
- DYH — Adhesive, Bracket And Tooth Conditioner, Resin
- Decision date
- 2023-12-01
- Date received
- 2023-06-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K231817
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.