Pro3Dure Medical GmbH

Pro3Dure Medical GmbH holds 4 FDA 510(k) medical device clearances, first cleared 2020, most recent 2022.

Top product codes for Pro3Dure Medical GmbH

Recent clearances by Pro3Dure Medical GmbH

K212017 — Thermeo SystemCode MQC·2022-04-08
K211415 — GR Splint Resin SystemCode MQC·2021-10-21
K210298 — GR-14 Resin SystemCode EBI·2021-05-05
K201827 — GR-17 Resin SystemCode EBG·2020-11-05

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