K242702
- 510(k) number
- K242702
- Device name
- VioSeal
- Applicant
- Spident Co., Ltd. KR
- Product code
- KIF — Resin, Root Canal Filling
- Decision date
- 2024-11-07
- Date received
- 2024-09-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K242702.pdf
Official FDA record: K242702
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.