510(k) K261710
K261710 is an FDA 510(k) premarket notification submitted by Apyx Medical Corporation for the device "AYON Power Liposuction Cannulas and AYON Power Liposuction Cannula Adaptors". The FDA issued a decision of Substantially Equivalent on August 21, 2026. The device falls under product code QPB (System, Suction, Lipoplasty For Removal), a Class II device regulated under 21 CFR 878.5040. Apyx Medical Corporation has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 21, 2026
- Date Received
- May 22, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Suction, Lipoplasty For Removal
- Device Class
- Class II
- Regulation Number
- 878.5040
- Review Panel
- SU
- Submission Type
A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring