Founded in 2002 and headquartered in Columbia, Maryland, with more than 300 employees in the United States, ACell, Inc. is a leading developer, manufacturer, and marketer of next-generation regenerative medicine products. ACell offers their regenerative medicine products through the development and commercialization of unique extracellular matrix medical devices to repair and remodel damaged tissues and organs in a broad range of surgical procedures.
ACell medical devices are cleared for a variety of indications and are marketed under the brand name "MatriStem." A privately held company, ACell produces MatriStem at its full scale manufacturing facilities in Columbia, MD and Lafayette, IN, and markets its products to physicians in the U.S. through a national direct sales force.
|
|
|
51-200 employees
View all ACell, Inc. employees
|
|
Medical Devices
|
|
6640 Eli Whitney Drive, Columbia, Maryland 21046, US
|
|
2002
|
|
Medical Devices, Regenerative Medicine, Extracellular Matrix Technology
|
Jim Defrancesco is the CEO of ACell, Inc..
The decision makers in ACell, Inc. are Barry Brainard, Barry Brainard, Brad Adams, etc. Click to Find ACell, Inc. decision makers emails.
ACell, Inc. specializes in regenerative medicine products that utilize extracellular matrix (ECM) technology. Their product line includes surgical implants, wound care solutions, and tissue repair products designed to promote healing and tissue regeneration. These products are primarily used in various medical fields, including orthopedics, urology, and general surgery.
ACell's extracellular matrix technology provides a natural scaffold for tissue regeneration. The ECM is derived from porcine bladder and is designed to mimic the body's own tissue environment. When implanted, it supports cellular infiltration and promotes the body's healing processes, allowing for the regeneration of new tissue while minimizing scarring and complications.
ACell's products are utilized across various medical fields, including but not limited to orthopedics, where they aid in bone and soft tissue repair; urology, for bladder and pelvic floor reconstruction; and general surgery, particularly in wound care and surgical site management. Their versatile ECM technology is applicable in multiple specialties, enhancing healing outcomes.
ACell's products are regulated by the U.S. Food and Drug Administration (FDA) and are classified as medical devices. The company ensures compliance with all regulatory requirements and maintains rigorous quality control processes to meet the standards set forth by the FDA. Many of their products have received 510(k) clearance, allowing them to be marketed and used in clinical settings.
Yes, ACell is committed to supporting healthcare professionals through comprehensive training and educational resources. They offer workshops, webinars, and on-site training sessions to ensure that medical practitioners are well-equipped to use their products effectively. Additionally, ACell's customer support team is available to assist with any inquiries or technical support needs.
To learn more about ACell's research and development initiatives, you can visit their official website, where they provide information on ongoing studies, clinical trials, and collaborations with academic institutions and healthcare organizations. ACell is dedicated to advancing regenerative medicine and frequently publishes updates on their innovations and findings in the field.
Find accurate personal emails, work emails and phone numbers for employees
Accelerate prospecting with instant access to 300M professionals from 30M companies with the right contact details.