Medical Device Manufacturer · US , Kennesaw , GA

Dornier Medtech America - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2013

6

Total

6

Cleared

0

Denied

Dornier Medtech America has 6 FDA 510(k) cleared medical devices. Based in Kennesaw, US.

Latest FDA clearance: Jan 2025. Active since 2013. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Dornier Medtech America Filter by specialty or product code using the sidebar.

6 devices

1–6 of 6

Hoover Negative Pressure Access Sheath (Hoover) (Hoover Model #'s IVX-NS-1040, IVX-NS-1050, IVX-NS-1140, IVX-NS-1150, IVX-NS-1240, IVX-NS-1250

K243820 · FED Endoscopic Access Overtube, Gastroenterology-urology · Gastroenterology & Urology

TRIDENT Mobile Fluoroscopy System

K233380 · JAA System, X-ray, Fluoroscopic, Image-intensified · Radiology

Dornier Medilas H Solvo 35 Laser

K180350 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery

Delta III Lithotripter

K170122 · LNS Lithotriptor, Extracorporeal Shock-wave, Urological · Gastroenterology & Urology

K151298 · LNS Lithotriptor, Extracorporeal Shock-wave, Urological · Gastroenterology & Urology

EXTRA CORPOREAL SHOCKWAVE LITHOTRIPTER

K132672 · LNS Lithotriptor, Extracorporeal Shock-wave, Urological · Gastroenterology & Urology