DeviceClearance

Product code LFL— Unknown

CUSA Clarity Ultrasonic Surgical Aspirator System

Classification name
Instrument, Ultrasonic Surgical
Device class
Unclassified
Advisory panel
Unknown
Total cleared
158
First cleared
Most recent

Market context for product code LFL

FDA has cleared 158 devices under product code LFL between 1980 and 2026, filed by 74 applicant companies. No FDA device recalls reference this product code.

Clearances per year

last 15 years

Top applicants under product code LFL

Adverse events under product code LFL

product code LFL
Death
29
Injury
1,046
Malfunction
21,642
Total
22,717

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code LFL

1–100 of 158

Data sourced from openFDA. This site is unofficial and independent of the FDA.