LFL

Instrument, Ultrasonic Surgical

Product code
LFL
Device name
Instrument, Ultrasonic Surgical
Device class
Class U
Medical specialty
Unknown
Marketing pathway
510(K)
510(k) clearances (last 3 years)
7
Summaries archived here
6 (direct download)
510(k) clearances (all years, FDA)
158 (all years; only the last 3 years are listed here)

510(k) clearances, last 3 years (7)

Last three years. Most recent: 2026-07-30.

NumberDecision dateApplicantDevice nameSummary
K2614482026-07-30Misonix, LLCneXus Ultrasonic Surgical Aspirator SystemPDF
K2511622025-10-08Integra LifeSciences CorporationCUSA® Clarity Ultrasonic Surgical Aspirator SystemPDF
K2428942025-06-18Shanghai Saints Sages Surgical Co., Lt…SanAgile™ Ultrasonic Surgery Advanced Portable Contr…PDF
K2439302025-03-24Stryker InstrumentsSonopet iQ Ultrasonic Aspirator System (5500-050-000…PDF
K2417002024-11-18Trice Medical, Inc.Tenex 2nd Generation SystemPDF
K2404932024-07-11Integra LifeSciences CorporationCUSA® Clarity Ultrasonic Surgical Aspirator SystemPDF
K2330362024-06-18Hunan Handlike Minimally Invasive Surg…Ultrasonic Surgical SystemFDA

6 summaries are archived here for direct download.

Official FDA classification page: LFL
Classification and pathway per current FDA publications. Data from openFDA (CC0).