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Neocis Guidance System (NGS) with Yomi Plan v2.0.1
FDA 510(k)Class II (US FDA 510(k))
510(k) K210711
by Neocis Inc
Identifiers
- 510(k) Number
- K210711 FDA 510(k)
- FDA Product Code
- PLV FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.4120 FDA 510(k)
- Regulation Number
- 872.4120 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Neocis Guidance System (NGS) with Yomi Plan v2.0.1 by Neocis Inc — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K210711 | Class II | Active |
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Manufacturer
- Manufacturer
- Neocis Inc
- FDA Applicant
- Neocis, Inc.
Sources (1)
- FDA 510(k) K210711 24 fields · synced Jun 19, 2026