K242383
- 510(k) number
- K242383
- Device name
- Apex Locator
- Applicant
- Shenzhen Rogin Medical Co., Ltd. CN
- Product code
- LQY — Locator, Root Apex
- Decision date
- 2025-03-07
- Date received
- 2024-08-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K242383.pdf
Official FDA record: K242383
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.