FDA cleared the Sonopet iQ Series III Console (5700-050-000); Sonopet iQ+ Straight Handpiece (5500-260-000); Sonopet iQ+ 10mm iQ+ Blade (5500-26B-010); Sonopet iQ+ 20mm iQ+ Blade (5500-26B-020); Sonopet iQ+ 11cm iQ+ Apex Knife (5500-26B-114); Sonopet iQ+ 12cm iQ+ Apex 360 (5500-26B-312); Sonopet iQ+ 12cm iQ+ Claw (5500-26B-328) from Stryker Instruments on Oct 8, 2026 under K262244, a traditional 510(k). The device falls under product code LFL, Instrument, Ultrasonic Surgical as a Class U device. The review panel was Unknown.
FDA logged the submission as received on Jul 1, 2026. The decision came 99 days later, longer than the 90 FDA-day review goal, which usually means at least one additional information request.
Stryker Instruments has 4 other decisions in the tracker over the last 12 months: K261959 (Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)), K261544 (Hydro Irrigation System), K253679 (Hydro Irrigation System), K252282 (SurgiCount+ System).