K222688
- 510(k) number
- K222688
- Device name
- The Trust
- Applicant
- Genoss Co., Ltd. KR
- Product code
- EKX — Handpiece, Direct Drive, Ac-Powered
- Decision date
- 2024-08-09
- Date received
- 2022-09-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K222688.pdf
Official FDA record: K222688
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.