Medical Device Manufacturer · US , Indianapolis , IN

Vortek Surgical, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007

Recent clearances: ENDODRAPE(TM), ENDODRAPE

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vortek Surgical, LLC General Hospital ✕

2 devices

1-2 of 2

Cleared Jul 21, 2008

General Hospital · 164d

Cleared Jul 30, 2007

General Hospital · 168d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 29, 2026