IC Surgical, Inc.


Medical technology company developing an internal negative-pressure wound control system consisting of an implantable multibranched internal conduit (manifold) and single-use portable therapy units. The company has conducted preclinical and clinical studies, maintains a patent portfolio, and is pursuing phased commercialization across plastic and general surgery indications.

Industries

health-care
medical-device
therapeutics

Nr. of Employees

small (1-50)


Patents

Adaptable wound drainage system

US-11878102-B2

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Adaptable wound drainage system

US-11638779-B2

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Assemblies, systems, and methods for vacuum assisted internal drainage during wound healing

US-10695469-B2

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Negative pressure pumps and related methods

US-10548778-B2

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Adaptable wound drainage system

US-10543300-B2

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Adaptable wound drainage system

US-10342901-B2

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Products

Internal negative-pressure wound control system (manifold + therapy unit)

A combined system comprising an implantable multibranched internal manifold conduit and single-use portable therapy units designed to apply continuous negative pressure to internal tissue planes and remove fluid postoperatively; supplied as configurable surgical kits.


Services

Provision of downloadable clinician and patient instructional materials, user guides, and educational videos to support device use and patient self-care.

Commercial ordering support and product information for hospital and clinic customers, including configurable perioperative kits and therapy unit packs.

Expertise Areas

  • Internal negative-pressure wound therapy
  • Clinical trial design and execution (pilot and retrospective studies)
  • Preclinical animal model studies (porcine)
  • Medical device design and system integration
  • Show More (4)

Key Technologies

  • Internal negative-pressure wound therapy
  • Multibranched internal manifold conduits
  • Single-use portable suction devices
  • One-way connector mechanisms
  • Show More (4)

News & Updates

Retrospective comparative study reporting statistically significant reductions in seroma, flap revision, any complication, and duration of therapy versus standard drains in prepectoral breast reconstruction (reported n=170 vs n=166 breasts).

Prospective pilot clinical study (n=24) evaluating safety and functionality of the internal negative-pressure system in abdominoplasty with no clinical seromas or device malfunctions reported through 30 days.

Clinical imaging evaluation using high-resolution ultrasound to assess internal tissue closure without fluid collection.

Independent publication reporting significant reductions in seroma and other complications versus standard drains in breast reconstruction patients.

24-patient pilot study in abdominoplasty demonstrating absence of clinical seroma and no device-related adverse events through 30 days.


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