FDA device listing
Lima PSI,Materialise Knee Guide planner,Materialise Knee Guides,Materialise Knee Guide System,Materialise Knee…
FDA device listing 1383155258 · MATERIALISE N.V.
Key facts
| Proprietary names | Lima PSI,Materialise Knee Guide planner,Materialise Knee Guides,Materialise Knee Guide System,Materialise Knee Planner,Materialise Knee Platform,Materialise SurgiCase Knee Module,Materialise SurgiCase Knee Planner,Materialise TKA Guide planner,Materialise TKA Guides,Materialise TKA Guide System,SurgiCase Knee Planner |
|---|---|
| Owner/operator | MATERIALISE N.V. |
| Owner/operator number | 9029485 |
| Premarket submissions | K162273 |
| Product codes | JWH, MBH, OIY, OOG |
| Device names | JWH - Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, MBH - Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer, OIY - Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive, OOG - Knee Arthroplasty Implantation System |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3560, 888.3565 |
| Review panels | Orthopedic |
| Registered establishments | MATERIALISE N.V., Materialise Sdn Bhd, Materialise Ukraine, Rep. office, Materialise USA, LLC. |
| Establishment registrations | 3003998208, 3005718816, 3009555440, 3009555447 |
| FEI numbers | 3003998208, 3005718816, 3009555440, 3009555447 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database