
At Beere, quality is instilled into every instrument we produce. Beere complies with FDA's Medical Device Quality System Regulation (21 CFR Part 820). Beere's Quality System is Certified to: ISO 13485:2003.
Beere is an approved supplier for over 300 domestic customers and 70 international customers.
As surgeons know, the human anatomy offers numerous constraint challenges. Beere instruments are designed and manufactured specifically to help reduce these obstacles. Each of these products, and the procedures in which they are used, are thoroughly researched to help minimize difficulties under trauma conditions. Beere engineers use their experience to produce some of the most innovative and advantageous instruments available.
Each Beere instrument has been put through an extensive research and development analysis. This affirms that nothing has been overlooked. After design criteria and performance standards have been determined, we utilize the latest CAD and modeling software to develop your product. Using the latest solid modeling software and onsite video conferencing greatly enhances our communication with our customers' engineering personnel. Communication is vital when jointly developing state-of-the-art instrumentation that meets the most demanding requirements of our customers.
Wherever possible, our products are developed in cooperation with the surgeon's input. Unique ergonomic handle designs reduce fatigue without sacrificing necessary feel and precision. We offer full service prototyping, clinical (pre-production), and production builds to meet your most demanding needs.
Beere is dedicated to using the highest quality autoclaveable, medically approved materials available. These materials are certified with full traceability in the finest grades of stainless steel, titanium, aluminum, super alloys, phenolic, silicone, and plastic.
Beere instruments are manufactured in our 68,000 square foot state-of-the-art manufacturing facility in Kenosha, Wisconsin.
