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 · Surgical robots · Investigated by FDA
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Sources (1)
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?
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: Verified · 1 source (1 primary) · last reviewed 2026-07-21
Verification posture
Verified
High confidence
Review state
Stable
Last reviewed 2026-07-21
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