
Share on:
Precision ADM, a contract manufacturer specializing in additive manufacturing (AM), is now registered in FDA’s Registration and Device Listing Database.
The designation confirms that Precision ADM meets standards set by FDA to manufacture medical devices.
“We’re very proud to be the only metal additive manufacturing service provider in Canada to hold ISO 13485 Certification and FDA establishment registration,” Chief Executive Officer Martin Petrak said in a press release. “This highlights our commitment to Quality Management Systems and to providing regulatory-approved devices to our clients.”
Along with AM, Precision ADM’s capabilities include subtractive multi-axis machining, design and testing services.
Source: Precision ADM
RELATED ARTICLES
Navigating the Road to Success in New Product Commercialization
Aug 25 2025 , BONEZONE Editors
Brightmark and Lewis Salvage Partnership Hits Major Milestone
Aug 12 2025 , Julie A. Vetalice
AddUp, OIC and Medi Mold Partner on 3D Printing in India
Aug 07 2025 , Julie A. Vetalice