Neocis, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neocis, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Yomi S Robotic System, Yomi Robotic System, Yomi Robotic System
18
Total
18
Cleared
0
Denied
Neocis, Inc. has 18 FDA 510(k) cleared dental devices. Based in Miami, US.
Latest FDA clearance: Oct 2025. Active since 2016.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neocis, Inc.
18 devices
Cleared
Oct 28, 2025
Yomi S Robotic System
Dental
90d
Cleared
Oct 10, 2025
Yomi Robotic System
Dental
116d
Cleared
Aug 14, 2023
Yomi Robotic System
Dental
126d
Cleared
Dec 08, 2022
Yomi Robotic System
Dental
87d
Cleared
Nov 04, 2022
Yomi Robotic System
Dental
115d
Cleared
Jun 14, 2022
Yomi Robotic System with YomiPlan Go
Dental
399d
Cleared
Dec 22, 2021
Neocis Guidance System (NGS) with Yomi Plan v2.0.1
Dental
287d
Cleared
Jul 28, 2021
Neocis Guidance System (NGS) with Intraoral Fiducial Array
Dental
103d
Cleared
Dec 15, 2020
Neocis Guidance System (NGS) with Patient Splints (EPS)
Dental
26d
Cleared
Dec 04, 2020
Neocis Guidance System (NGS) with Yomi Plan v2.0
Dental
115d
Cleared
Oct 19, 2020
Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)
Dental
82d
Cleared
Jul 28, 2020
Neocis Guidance System (NGS) with Patient Splints
Dental
123d