Dornier Medtech America Inc (Dmta)

Dornier Medtech America Inc (Dmta) holds 1 FDA 510(k) medical device clearance, cleared in 2025.

Top product codes for Dornier Medtech America Inc (Dmta)

FAS — Gastroenterology, Urology1 device

Recent clearances by Dornier Medtech America Inc (Dmta)

K251403 — Dornier Bi-Polar Electrode BIP12CLM Bipolar 12° Medium Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP12CLL Bipolar 12° Large Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP30CLM Bipolar 30° Medium Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP30CLL Bipolar 30° Large Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIPMBLA Bipolar Medium Bladder Loop 24 Fr Electrode-Sterile, Single-Use BIPNEEL Bipolar Needle 24 Fr Electrode-Sterile, Single-Use BIPDDSC Bipolar Disc )Code FAS·2025-12-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.