FDA 510(k) clearance · back to tracker

Yomi S Robotic System

Neocis, Inc. cleared K261321 on 2026-10-13, decision: substantially equivalent

K-number

K261321

Sponsor

Neocis, Inc.

Device

Yomi S Robotic System

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-10-13

Product code

QRY

Advisory committee

Dental

Medical specialty

Dental

Regulation number

872.4120

Official FDA record

Open K261321on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.