Yomi S Robotic System
K-Number: K252376 · 2025-10-28
Device Summary
Frequently Asked Questions
What is the Yomi S Robotic System?
Yomi S Robotic System is a medical device that received FDA 510(k) clearance on 2025-10-28. The listed applicant is Neocis, Inc.. The 510(k) number is K252376.
When did Yomi S Robotic System receive FDA 510(k) clearance?
Yomi S Robotic System received FDA 510(k) clearance on 2025-10-28, under 510(k) number K252376.
Who is the listed applicant for Yomi S Robotic System?
The FDA 510(k) record lists Neocis, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Yomi S Robotic System?
The FDA product code for Yomi S Robotic System is PLV.
Other records listing Neocis, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: PLV)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.