Product code LFD— Unknown

NEUTRASAL

Classification name
Saliva, Artificial
Device class
Unclassified
Advisory panel
Unknown
Total cleared
50
First cleared
Most recent

Market context for product code LFD

FDA has cleared 50 devices under product code LFD between 1981 and 2026, filed by 40 applicant companies. No FDA device recalls reference this product code.

Clearances per year

last 15 years

Top applicants under product code LFD

Adverse events under product code LFD

product code LFD
Death
3
Total
3

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 LFD

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