Leaders in Regulatory Affairs for the Medical Device Industry

Monthly Archives: April 2016

For Immediate Release:

PaxMed proudly announces the FDA clearance of the Blue Sky Bio Zygomatic Implant System 510(k) submission. This marks the 184th clearance for PaxMed, the 41st clearance for Dr. Kevin A. Thomas, Vice President and Director of Regulatory Affairs.

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PaxMed Proudly Announces Its 183rd 510(k) Clearance

For immediate release: March 30, 2016 On behalf of Camlog (Altatec GmbH), PaxMed International announces the FDA clearance of the Abutment for Bridges 510(k). This marks PaxMed’s 183rd clearance and the 56th clearance for our Senior Regulatory Specialist, Linda Schulz.

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