Dornier Medtech America
Dornier Medtech America holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2025.
Top product codes for Dornier Medtech America
Recent clearances by Dornier Medtech America
- K243820 — 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
- K233380 — TRIDENT Mobile Fluoroscopy System
- K180350 — Dornier Medilas H Solvo 35 Laser
- K170122 — Delta III Lithotripter
- K151298 — Gemini XXP-HP
- K132672 — EXTRA CORPOREAL SHOCKWAVE LITHOTRIPTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.