Medical Device Manufacturer · US , San Clamente , CA

Vertiflex, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2008

Total

Cleared

Denied

Vertiflex, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Clamente, US.

Historical record: 5 cleared submissions from 2008 to 2012. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Vertiflex, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vertiflex, Inc.

5 devices

1-5 of 5