GIG HARBOR, Wash.--(BUSINESS WIRE)--Generic Medical Devices, Inc.™ (GMD™), the first company to design, develop, manufacture and supply quality surgical products marketed at generic prices, today announced that the U.S. Food and Drug Administration (FDA) has cleared the GMD Universal Surgical Mesh for market. This marks the company’s second 510(k) clearance by the FDA for a medical device that will be sold as a generic alternative to existing, standard-of-care surgical products. The availability of the Surgical Mesh will provide hospitals, ambulatory surgical centers, and independent practitioners a low-cost opportunity to administer high-quality healthcare.
