Momentis Surgical , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Momentis Surgical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Anovo Surgical System (Model 6Ne), Anovo Surgical System (6Ne), Anovo Instrument ARM Curved Scissors
9
Total
8
Cleared
1
Denied
Momentis Surgical , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Or Yehuda, IL.
Latest FDA clearance: Jul 2026. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Momentis Surgical , Ltd. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Momentis Surgical , Ltd.
9 devices
Cleared
Jul 22, 2026
Anovo Surgical System (6Ne)
General & Plastic Surgery
132d
Cleared
Jul 08, 2025
Anovo Surgical System (Model 6Ne)
General & Plastic Surgery
29d
Cleared
Jun 06, 2025
Anovo Surgical System (6Ne)
General & Plastic Surgery
99d
Cleared
May 02, 2025
Anovo Instrument ARM Curved Scissors
General & Plastic Surgery
28d
Cleared
Feb 03, 2025
Anovo Instrument ARM Curved Scissors
General & Plastic Surgery
126d
Cleared
Oct 21, 2024
Anovo Surgical System (Model 6Ne)
General & Plastic Surgery
90d
Cleared
CT
Oct 02, 2024
Anovo Surgical System (model 6N)
General & Plastic Surgery
93d
Cleared
Sep 14, 2023
Anovo Pedestal
General & Plastic Surgery
57d
Not Cleared
Feb 26, 2021
Hominis Surgical System
General & Plastic Surgery
681d