Momentis Surgical , Ltd.

FDA Regulatory Profile

Momentis Surgical , Ltd. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 8, 2025.

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251761Anovo Surgical System (Model 6Ne); Anovo Instrument ARM Curved Scissors ; Anovo Instrument ARM Hook July 8, 2025
K250591Anovo Surgical System (6Ne)June 6, 2025
K251056Anovo Instrument ARM Curved Scissors ; Anovo Instrument ARM Hook ElectrodeMay 2, 2025
K243182Anovo Instrument ARM Curved Scissors; Anovo Instrument ARM Hook ElectrodeFebruary 3, 2025
K242157Anovo Surgical System (Model 6Ne)October 21, 2024
K241907Anovo Surgical System (model 6N)October 2, 2024
K232146Anovo PedestalSeptember 14, 2023
DEN190022Hominis Surgical SystemFebruary 26, 2021