Salona Global's plan is developing a heavily integrated, IP driven vertical infrastructure spread across several facilities.
With each acquisition Salona Global anticipates that its international presence, IP, revenue, cash flow, and infrastructure will grow. Stay tuned for the next facility to be integrated into the Salona Global Family of Products.
San Diego, CA
The corporate headquarters in San Diego, California is at the robust heart of a leading city in the US medical device industry. This prime Southern California location allows management easy interface with medical device leaders from around the globe. With centralized accounting, finance, human resources and executive oversight, the Corporate Office is where the strategy and value of Salona Global is germinated.
South Dakota Partners (SDP)
The first acquisition of the Salona Global growth strategy, SDP has extensive development, research and production capabilities at its state of the art FDA approved facility located in Clearlake, South Dakota. Currently SDP develops and manufactures white label medical devices for an array of global businesses. Clearlake offers a strong foundation on which Salona Global can develop.
Specialty Design and Customization
SDP has developed the capability to customize the entire development pipeline of white labeled medical devices. From CNC machining to ultrasonic welding and kitting, SDP is prepared for every step of the process.
Engineering and Development
With nearly a century of collective work years among them, the five members of the Engineering and Development team are responsible for innovation of new devices and optimization of existing technologies and work flows.
Rework and Warranty Service
SDP offers IPC level rework and repair of our manufactured products allowing for improved service on and innovation of the medical devices manufactured onsite.
SDP is fully built out and realized for all stages of customization, programming, testing and distributing our custom medical devices.
Clear Lake Capabilities
SDP's state-of-the-art Clearlake facility is registered by the FDA in compliance with US and FDA standards. It boasts multiple automated lines throughout its large product floor. With automated SMT, selective soldering and PCBA capability, it can produce an astounding breadth of medical devices.
With over 30 years of medical device and product development history, the Clearlake facility is a quintessential American medical device plant. The facility is certified to the highest industry standards including ISO 13485 and IPC-A-610 and is RoHS compliant.
The facility has an extensive development and innovation center that custom designs the manufacturing process for speed and quality with maximum automation and speed.
More coming soon...