FDA device listing
DURACON; DURACON PRESSFIT STEM COCR; EXETER INTRAMEDULLARY BONE PLUG; TI DURACON REG FLUTED STEM
FDA device listing 1206606188 · Nelipak Healthcare Packaging
Key facts
| Proprietary names | DURACON; DURACON PRESSFIT STEM COCR; EXETER INTRAMEDULLARY BONE PLUG; TI DURACON REG FLUTED STEM |
|---|---|
| Owner/operator | Nelipak Healthcare Packaging |
| Owner/operator number | 9082522 |
| Product codes | MBH |
| Device names | MBH - Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3565 |
| Review panels | Orthopedic |
| Registered establishments | Nelipak Healthcare Packaging |
| Establishment registrations | 3005581234 |
| FEI numbers | 3005581234 |
| Establishment operations | Contract Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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