Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Neocis Inc. with 19 510(k) clearances and 5 device recalls. The most recent is a 510(k) clearance dated Oct 13, 2026: Yomi S Robotic System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Oct 13, 2026 | Yomi S Robotic SystemK261321 · QRY | 510(k) clearances |
| Oct 28, 2025 | Yomi S Robotic SystemK252376 · PLV | 510(k) clearances |
| Oct 10, 2025 | Yomi Robotic SystemK251835 · PLV | 510(k) clearances |
| Aug 14, 2023 | Yomi Robotic SystemK231018 · PLV | 510(k) clearances |
| Dec 8, 2022 | Yomi Robotic SystemK222750 · QRY | 510(k) clearances |
| Nov 4, 2022 | Yomi Robotic SystemK222049 · QRY | 510(k) clearances |
| Jun 14, 2022 | Yomi Robotic System with YomiPlan GoK211466 · PLV | 510(k) clearances |
| Dec 22, 2021 | Neocis Guidance System (NGS) with Yomi Plan v2.0.1K210711 · PLV | 510(k) clearances |
| Oct 30, 2020 | DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent system, the Neocis Guidance System (NGSClass II · The LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled. | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
