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Medtronic Wins FDA Clearance for LigaSure RAS Maryland on Hugo Robot

What happened

Medtronic has submitted 510(k) filings to the FDA seeking clearance for its Hugo robotic-assisted surgery system to be used in general surgery and gynecologic surgery.

Source

Article excerpt

Medtronic announced on September 16, 2026, that the U.S. Food and Drug Administration (FDA) has cleared the LigaSure RAS Maryland jaw device for use with the Hugo robotic-assisted surgery (RAS) system. The clearance expands the instrument lineup available on the Hugo system for U.S. robotic-assisted procedures. According to Medtronic, the LigaSure RAS Maryland is built to work only with the Valleylab FT10 energy platform on the Hugo RAS system. The company said the instrument seals and cuts vessels, thick tissue, and lymphatics up to and including 7 mm in diameter, and that it seals vessels in approximately 2 seconds while limiting thermal spread to surrounding tissue. Medtronic describes the LigaSure RAS Maryland as the first robotically driven LigaSure instrument, and said the vessel-sealing technology it incorporates has been used in more than 45 million procedures across more than 65 countries over the past two decades. The instrument was introduced on the Hugo RAS system in Europe in 2025 following CE Mark. Medtronic’s product page for the device states that the jaw vessel sealer has reached the U.S. market, and describes it as pairing ValleyLab FT10 generator sealing with the versatility of the Hugo RAS system. The Hugo RAS system is cleared in the U.S. for urologic surgical procedures and, according to the company, is in commercial use at a growing number of health...

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Extracted from this sentence

In a June 3, 2026 announcement , Medtronic said it had submitted 510(k) filings to the FDA seeking clearance for Hugo system use in general surgery, including hernia repair, and in gynecologic surgery.

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From the Signal API record
Event
In development

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Product
Hugo RAS system
Location
United States

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The full record

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Topics and mentions

Product tags

  • general technology
  • medical

Extraction

Confidence
90%
Detected
Sep 16, 2026
signal_type
news
signal_subtype
is_developing

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This page shows a preview. The full news record in the Signal API and MCP can also have these 8 fields. Some fields are empty for some signals.

Company

  • linkedin_urlValue in the API
  • industriesValue in the API
  • employee_count_lowValue in the API
  • employee_count_highValue in the API
  • revenueValue in the API
  • descriptionValue in the API

Signal

  • signal_nameValue in the API
  • associationValue in the API
Show the full JSONThe record on this page and the API request

GET /v1/signals/26c477f6-a3d9-38d6-1de6-b864c498d43d returns this record as JSON. POST /v1/companies/enrich returns every signal for medtronic.com.

{
  "signal_id": "26c477f6-a3d9-38d6-1de6-b864c498d43d",
  "signal_type": "news",
  "signal_subtype": "is_developing",
  "detected_at": "2026-09-16T11:02:01+00:00",
  "company": {
    "name": "Medtronic",
    "domain": "medtronic.com"
  },
  "data": {
    "url": "https://www.unite.ai/medtronic-wins-fda-clearance-for-ligasure-ras-maryland-on-hugo-robot/",
    "title": "Medtronic Wins FDA Clearance for LigaSure RAS Maryland on Hugo Robot - Unite.AI",
    "excerpt": "Medtronic announced on September 16, 2026, that the U.S. Food and Drug Administration (FDA) has cleared the LigaSure RAS Maryland jaw device for use with the Hugo robotic-assisted surgery (RAS) system. The clearance expands the instrument lineup available on the Hugo system for U.S. robotic-assisted procedures. According to Medtronic, the LigaSure RAS Maryland is built to work only with the Valleylab FT10 energy platform on the Hugo RAS system. The company said the instrument seals and cuts vessels, thick tissue, and lymphatics up to and including 7 mm in diameter, and that it seals vessels in approximately 2 seconds while limiting thermal spread to surrounding tissue. Medtronic describes the LigaSure RAS Maryland as the first robotically driven LigaSure instrument, and said the vessel-sealing technology it incorporates has been used in more than 45 million procedures across more than 65 countries over the past two decades. The instrument was introduced on the Hugo RAS system in Europe in 2025 following CE Mark. Medtronic’s product page for the device states that the jaw vessel sealer has reached the U.S. market, and describes it as pairing ValleyLab FT10 generator sealing with the versatility of the Hugo RAS system. The Hugo RAS system is cleared in the U.S. for urologic surgical procedures and, according to the company, is in commercial use at a growing number of health...",
    "product": "Hugo RAS system",
    "summary": "Medtronic has submitted 510(k) filings to the FDA seeking clearance for its Hugo robotic-assisted surgery system to be used in general surgery and gynecologic surgery.",
    "location": "United States",
    "planning": false,
    "image_url": "https://www.unite.ai/wp-content/uploads/2026/09/medtronic-wins-fda-clearance-for-ligasure-ras-maryland-on-hugo-robot.jpg",
    "confidence": 0.9,
    "product_data": {
      "name": "Hugo RAS system",
      "full_text": "Hugo robotic-assisted surgery (RAS) system",
      "fuzzy_match": false
    },
    "product_tags": [
      "general_technology",
      "medical"
    ],
    "published_at": "2026-09-16T11:02:01Z",
    "location_data": [
      {
        "region": "Northern America",
        "country": "United States",
        "continent": "Americas",
        "fuzzy_match": false
      }
    ],
    "article_sentence": "In a June 3, 2026 announcement , Medtronic said it had submitted 510(k) filings to the FDA seeking clearance for Hugo system use in general surgery, including hernia repair, and in gynecologic surgery."
  }
}

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