# Neocis, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 19 (2016–2026): 19 510(k) clearances
- Product codes: PLV (16), QRY (3)
- 510(k) review time since 2016: median 101 days, against 86 for FDA's reviews in the same codes and years (3 of 8 faster)
- Predicates its devices cite: 18 (16 its own); citations of its devices by later devices: 16 (16 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- X-Nav Technologies, LLC: 2 (https://510kreport.com/company/x-nav-technologies)

## Its most-cited devices
- K173402: Neocis Guidance System (NGS) with Chairside Splint (2018), cited by 3
- K161399: Neocis Guidance System (2016), cited by 3
- K202264: Neocis Guidance System (NGS) with Yomi Plan v2.0 (2020), cited by 2
- K231018: Yomi Robotic System (2023), cited by 2
- K182776: Neocis Guidance System (2018), cited by 2
- K200805: Neocis Guidance System (NGS) with Patient Splints (2020), cited by 1

## Recent decisions
- K261321: Yomi S Robotic System (Oct 13, 2026)
- K252376: Yomi S Robotic System (Oct 28, 2025)
- K251835: Yomi Robotic System (Oct 10, 2025)
- K231018: Yomi Robotic System (Aug 14, 2023)
- K222750: Yomi Robotic System (Dec 8, 2022)
- K222049: Yomi Robotic System (Nov 4, 2022)
- K211466: Yomi Robotic System with YomiPlan Go (Jun 14, 2022)
- K210711: Neocis Guidance System (NGS) with Yomi Plan v2.0.1 (Dec 22, 2021)

Source page: https://510kreport.com/company/neocis