ISO 13485 Certified, FDA Registered, Rose Technologies, Inc. As a Custom Medical Device Contract Manufacturer, Rose Technologies has the Engineering expertise to meet your entire medical device design, manufacturing, assembly, automation, and packaging needs. Whether you need short-term pilot runs, or long-term production in our class 10,000 clean rooms. The Rose Technologies' product/manufacturing Team of Engineers can provide prototypes, or a complete turnkey package for your new product.
We are an FDA registered contract medical device manufacturer and we are ISO 13485:2003 Certified. Our Quality system is based on the FDA's Quality System Regulation. We continue to impress new and existing customers during supplier audits. We are your Single-Source Medical Device supplier and we want to partner with you for your next new Medical Device.
Catalent offers a full range of development services, such as pre-clinical support, API development, analytical services, drug delivery development, clinical manufacturing and packaging services. We have expertise in inhalation development, and can offer innovative biologic cell-line development...
We have developed extensive capabilities with laryngeal mask airways, diagnostic devices, drug delivery systems, enteral feeding catheters, infusion sets, wire reinforced tubes, optically clear components, patient monitoring devices and other specialty products. Each of our locations has state...
We have 3 certified class 10,000 clean rooms, one of which is specifically designed and controlled for processing silicone components. Our specialties are: Dip molded balloon cuffs, assemblies with cuffs, wire reinforced silicone Cannula bodies, single and multi lumen tubes with inner diameters... Read more
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