Company · DE
Pro3Dure Medical GmbH
FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2026. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 29, 2026 | K260031 | THERMEO® I MSI Pro3Dure Medical GmbH, DE | MQC |
| Aug 8, 2024 | K231775 | GR Resin System MSI Pro3Dure Medical, DE | MQC |
| Apr 8, 2022 | K212017 | Thermeo System Pro3Dure Medical GmbH, DE | MQC |
| Oct 21, 2021 | K211415 | GR Splint Resin System Pro3Dure Medical GmbH, DE | MQC |
| May 5, 2021 | K210298 | GR-14 Resin System Pro3Dure Medical GmbH, DE | EBI |
| Nov 5, 2020 | K201827 | GR-17 Resin System Pro3Dure Medical GmbH, DE | EBG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||