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Incident · Regulatory action

FDA grants 510(k) clearance to Momentis Surgical Anovo system for multiport surgery, first platform supporting all three surgical access approaches

The U.S. FDA granted 510(k) clearance for the multiport configuration of Momentis Surgical's Anovo Surgical System on July 23, 2026. The clearance makes Anovo the first robotic surgical platform capable of supporting natural orifice, single-port, and multiport procedures on a single system, expanding the platform beyond its previously cleared indications.

Occurred 2026-07-23 · Momentis Surgical · 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 (2)

  1. PR Newswire · https://www.prnewswire.com/news-releases/fda-clears-momentis-surgicals-anovo-system-for-multiport-surgery-making-it-the-first-robotic-platform-to-support-three-surgical-approaches-302833131.html · 2026-07-23
  2. MassDevice · https://www.massdevice.com/fda-clears-momentis-multi-port-robot/ · 2026-07-23

Status history

  • Active · 2026-07-25 · agent:recon

Common questions

What happened in FDA grants 510(k) clearance to Momentis Surgical Anovo system for multiport surgery, first platform supporting all three surgical access approaches?
The U.S. FDA granted 510(k) clearance for the multiport configuration of Momentis Surgical's Anovo Surgical System on July 23, 2026. The clearance makes Anovo the first robotic surgical platform capable of supporting natural orifice, single-port, and multiport procedures on a single system, expanding the platform beyond its previously cleared indications.
When did this incident occur?
The incident is recorded as occurring on July 23, 2026 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in FDA grants 510(k) clearance to Momentis Surgical Anovo system for multiport surgery, first platform supporting all three surgical access approaches?
The incident is recorded as involving Momentis Surgical on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to FDA grants 510(k) clearance to Momentis Surgical Anovo system for multiport surgery, first platform supporting all three surgical access approaches?
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 grants 510(k) clearance to Momentis Surgical Anovo system for multiport surgery, first platform supporting all three surgical access approaches?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Verified · 2 sources (no primary) · last reviewed 2026-08-09

Verification posture

Verified

Low confidence

Review state

Stable

Last reviewed 2026-08-09

Sources by quality tier

2
unclassified
Unclassified source

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

Methodology surface for FDA grants 510(k) clearance to Momentis Surgical Anovo system for multiport surgery, first platform supporting all three surgical access approaches.

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Canonical ID 1570fb0f-67fb-4ebe-b081-e3efd981a58d