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Incident · Regulatory action

ROBODOC Surgical System receives FDA 510(k) marketing clearance

DigiMatch n ROBODOC Surgical System received FDA 510(k) marketing clearance for its orthopedic surgical robot platform.

Occurred 2026-06-30 · ROBODOC · Investigated by FDA

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Incident records on DEPLOY are compiled from public sources (regulatory filings, news reports, and operator disclosures) and reflect what has been reported and tracked to date. They are not legal findings, determinations of fault, or safety ratings, and may be updated as new information is verified. See the sources below for the underlying references.
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Sources (1)

  1. https://www.biospace.com/digimatch-tm-n-robodoc-surgical-system-receives-u-s-fda-510-k-marketing-clearance

Status history

  • Active · 2026-07-03 · agent:depth

Common questions

What happened in ROBODOC Surgical System receives FDA 510(k) marketing clearance?
DigiMatch n ROBODOC Surgical System received FDA 510(k) marketing clearance for its orthopedic surgical robot platform.
When did this incident occur?
The incident is recorded as occurring on June 30, 2026 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in ROBODOC Surgical System receives FDA 510(k) marketing clearance?
The incident is recorded as involving ROBODOC on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to ROBODOC Surgical System receives FDA 510(k) marketing clearance?
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 ROBODOC Surgical System receives FDA 510(k) marketing clearance?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Verified · 1 source (no primary) · last reviewed 2026-07-14

Verification posture

Verified

Low confidence

Review state

Stable

Last reviewed 2026-07-14

Sources by quality tier

1
unclassified
Unclassified source

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

Methodology surface for ROBODOC Surgical System receives FDA 510(k) marketing clearance.

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Canonical ID 65a3cd51-917a-482b-be0b-b49867c3483d