K260522
- 510(k) number
- K260522
- Device name
- RhinAer+ Stylus
- Applicant
- Aerin Medical, Inc. CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-05-18
- Date received
- 2026-02-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K260522.pdf
Official FDA record: K260522
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.