K242675
- 510(k) number
- K242675
- Device name
- FineEtch (FineEtch-10 1.2ml, FineEtch-10 5ml, FineEtch-37 1.2ml FineEtch-37 5ml, FineEtch 37% 1.2ml 20ea pack)
- Applicant
- Spident Co., Ltd. KR
- Product code
- KLE — Agent, Tooth Bonding, Resin
- Decision date
- 2024-11-01
- Date received
- 2024-09-06
- 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: K242675.pdf
Official FDA record: K242675
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.