Medical Device Manufacturer · US , Research Triangle Park , NC

Weck Closure Systems - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Total

Cleared

Denied

Weck Closure Systems has 6 FDA 510(k) cleared medical devices. Based in Research Triangle Park, US.

Historical record: 6 cleared submissions from 1998 to 2001. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Weck Closure Systems Filter by specialty or product code using the sidebar.

Weck Closure Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Weck Closure Systems

6 devices

1-6 of 6