Medical Device Manufacturer · US , Carlsbad , CA

Vertiflex (Tm), Incorporated - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Vertiflex (Tm), Incorporated has 2 FDA 510(k) cleared medical devices. Based in Carlsbad, US.

Historical record: 2 cleared submissions from 2007 to 2007. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Vertiflex (Tm), Incorporated

2 devices

1-2 of 2