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.

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.

Incident · Injury

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.

Occurred 2024-01-01 · Yomi S · Neocis

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

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Data documentation: /data
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Sources (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.

Methodology: Unreviewed · 1 source (1 primary) · last reviewed 2026-07-04

Verification posture

Unreviewed

Low confidence

Review state

Stable

Last reviewed 2026-07-04

Sources by quality tier

1: primary-fda-database; FDA database

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

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