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Incident · Regulatory action

Revolve Surgical receives FDA 510(k) clearance for surgical robot platform

Revolve Surgical received FDA 510(k) clearance for its surgical robot platform. The Canada-based company develops a surgical robot for minimally invasive procedures.

Occurred 2026-06-15 · Revolve Surgical

Track Revolve Surgical receives FDA 510(k) clearance for surgical robot platform

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Sources (1)

  1. https://www.massrobotics.org/revolve-surgical-wins-fda-clearance-for-surgical-robot/

Status history

  • Active · 2026-07-03 · agent:depth

Common questions

What happened in Revolve Surgical receives FDA 510(k) clearance for surgical robot platform?
Revolve Surgical received FDA 510(k) clearance for its surgical robot platform. The Canada-based company develops a surgical robot for minimally invasive procedures.
When did this incident occur?
The incident is recorded as occurring on June 15, 2026 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in Revolve Surgical receives FDA 510(k) clearance for surgical robot platform?
The incident is recorded as involving Revolve Surgical on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to Revolve Surgical receives FDA 510(k) clearance for surgical robot platform?
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 Revolve Surgical receives FDA 510(k) clearance for surgical robot platform?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Unreviewed · 1 source (no primary) · last reviewed 2026-07-03

Verification posture

Unreviewed

Low confidence

Review state

Stable

Last reviewed 2026-07-03

Sources by quality tier

1
unclassified
Unclassified source

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

Methodology surface for Revolve Surgical receives FDA 510(k) clearance for surgical robot platform.

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Canonical ID d0a1a82c-3876-4714-81b1-cfe5acee7152