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Vascutek - Company History
Vascutek is a leading manufacturer of vascular prostheses, which are used worldwide by vascular and cardiovascular surgeons in the treatment of aneurysmal or occlusive arterial disease.


Based at a custom built factory in Inchinnan, adjacent to Glasgow Airport and currently employing over 250 personnel, Vascutek is engaged in the research, design, development and manufacture of an extensive range of sealed and unsealed polyester and ePTFE grafts, primarily utilizing its unique surface and gelatin impregnation technology to address the needs of vascular and cardiovascular surgeons.

Vascutek manufactures a wide range of sealed knitted polyester grafts for example, Gelseal™, Gelsoft™, Gelsoft™ Plus and a sealed woven polyester namely, Gelweave™. The ePTFE range consists of two gelatin sealed ranges, SEALPTFE™ and Taperflo™ plus a range of unsealed ePTFE and MAXIFLO™. These products are internationally recognized for their high quality and innovative design.

Vascutek is a global company with operations in more than 80 countries. This network supports the needs of healthcare professionals worldwide.

At present, over 90% of all production is exported – the company has won 4 Queen’s Awards for export achievement in 1988, 1990, 1993 and 1998, together with a Queen’s Award for Technological Achievement in 1988.

Vascutek is the market leader in Japan, the U.K. and many European countries. Recognition for achieving substantial sales in Japan was made with the company receiving an export award in 1992 from the Japanese External Trade Organisation (JETRO).

Vascutek launched Gelweave™ in 1992. This coincided with the company gaining approval in Japan for Gelsoft™. This increased sales by 47% versus 1991.

Our entry into the sealed graft market in the United States took place in 1993 when the company received FDA approval for Gelseal™. This was followed in 1995 with the introduction of Gelsoft™, thus allowing the company to successfully promote these knitted polyester grafts. Vascutek’s compliance with the FDA GMP requirements and with the Medical Devices Directive has allowed Vascutek to become one of the first medical device manufacturers to affix the CE mark to their products.

1996 saw the launch of a new fluoropolymer/polyester composite prosthesis, Fluoropassiv™. The patented Fluoropassiv™ technology has a unique fluoropolymer coating, resulting in lowered thrombogenicity and enhanced healing properties.

Vascutek’s continuing commitment to research and development culminates in a number of newly developed products that are moving into the clinical phase and will serve to maintain the company’s competitive edge in the future.

Vascutek’s pursuit of excellence and its commitment to "Quality, Innovation and Service" remain to the fore.