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Liquid Silicone Rubber Injection Molding

Why liquid silicone rubber (LSR) is a great material for producing medical components using injection molding?

Liquid Silicone Rubber Injection Molding has been steadily gaining a foothold in many markets due to its ability to produce intricate elastomeric components with relatively short cycle times. The automotive industry employs silicone high degradation temperatures for engine sealing and medical markets rely on silicone for its biological inertness.  Liquid Silicone Rubbers (LSRs) can be processed using slightly modified thermoplastic molding equipment, making them easy to integrate into existing business structures and facilities.

  • Material Description
  • Process Description
  • Process History and Development
  • Advantages/Disadvantages
  • Application Areas

Download our whitepaper to learn more about the capabilities of liquid silicone rubber injection molding.  It gives medical device manufacturers a complete guide to the advantages of liquid silicone molding and why silicone is a good material choice for your project.

About Saint-Gobain

Saint-Gobain designs, manufactures and distributes materials and solutions which are key ingredients in the wellbeing of each of us and the future of all. They can be found everywhere in our living places and our daily life: in buildings, transportation, infrastructure and in so many industrial applications.

 

Saint-Gobain Performance Plastics' group of businesses gather solutions to save energy, provide protection, improve comfort and sustain the environment for a variety of markets.

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Saint-Gobain’s medical products are distributed exclusively to medical device manufacturers for use in the manufacture, assembly or distribution of their medical devices. Saint-Gobain cannot authorize the sale of its medical products directly to device user facilities (e.g. hospitals, surgery centers, nursing home, clinics, etc.), nor directly to end users (e.g. patients, patients’ caregiver, prescribing physician, nurse, pharmacist, etc.), including distributors serving device user facilities and end users directly. In accordance with every jurisdiction globally, Saint-Gobain’s customers are responsible for determining that any medical device they manufacture and market that incorporates a Saint-Gobain’s medical product, is compliant with each country-specific medical device regulations and has received proper country-specific clearance, certification or registration authorizing the sale of this medical device.


Saint-Gobain’s medical products offer covers:
- Medical Components [21 CFR 820.3(c)], intended for processing or use in the manufacture or assembly of medical devices before the finished medical device is packaged/labeled; Medical Components are intended to be included as part of the finished, packaged, and labeled device [21CFR820.3(c)].
- Finished Devices [21CFR820.3(l)] made on behalf of medical device manufacturers [21 CFR 807.20(a)(2)] under contract-manufacturing agreement. In accordance with the United States’ jurisdiction, Saint-Gobain complies with the FDA’s requirements for contract manufacturers of finished devices.

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