_Incident · Injury_

# FDA MAUDE report: Yomi guided dental implant robot serious injury event

Canonical ID: `30ca7f19-5363-49fc-b145-27020b52e9f2`

- **Occurred:** 2024-01-01
- **Kind:** `injury`
- **Status (derived):** active
- **Model:** [Yomi S](/models/yomi-s.md) (id: `63feef63-412c-4520-93b6-8ffa1a826c6b`)
- **Company:** [Neocis](/companies/neocis.md) (id: `6502bb45-7c3f-4e3b-ad1f-5c0fe1738696`)

An adverse event report was filed in the FDA MAUDE database for the Neocis Yomi Guided Dental Implant Robot, classified as a serious injury. Details are limited in the public MAUDE filing.

## Sources (1)

1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=18783685&pc=QRY

## Status history

- **active** · 2026-07-04 · agent:depth

## Common questions

### What happened in FDA MAUDE report: Yomi guided dental implant robot serious injury event?

An adverse event report was filed in the FDA MAUDE database for the Neocis Yomi Guided Dental Implant Robot, classified as a serious injury. Details are limited in the public MAUDE filing.

### When did this incident occur?

The incident is recorded as occurring on January 1, 2024 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.

### What robot was involved in FDA MAUDE report: Yomi guided dental implant robot serious injury event?

Yomi S by Neocis is the recorded robot involved in this incident.

### Has anyone responded to FDA MAUDE report: Yomi guided dental implant robot serious injury event?

No responses to this incident are recorded on the DEPLOY registry. Operators, manufacturers, or affected parties can submit responses to the editorial team; absence is not a guarantee no response was issued.

### What is the current status of FDA MAUDE report: Yomi guided dental implant robot serious injury event?

This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.


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