Neurophet., Inc.

FDA Regulatory Profile

Neurophet., Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 15, 2026.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252563Neurophet SCALE PETMay 15, 2026
K261273Neurophet AQUAMay 15, 2026
K252496Neurophet AQUA AD PlusJan 29, 2026
K242215Neurophet AQUA (V3.1)Oct 25, 2024
K220437Neurophet AQUAMay 10, 2023
K221405Neurophet SCALE PETAug 5, 2022