FDA device listing
VIVACIT-E VITAMIN E HIGHLY CROSSLINKED POLYETHYLENE LINERS
FDA device listing 1202822097 · LYNX Medical Pennsylvania
Key facts
| Proprietary names | VIVACIT-E VITAMIN E HIGHLY CROSSLINKED POLYETHYLENE LINERS |
|---|---|
| Owner/operator | LYNX Medical Pennsylvania |
| Owner/operator number | 10094665 |
| Product codes | JDI, LPH, LZO, OQG, OQH, OQI |
| Device names | JDI - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented, LPH - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, LZO - Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented, OQG - Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented, OQH - Hip, Semi-Constrained, Cemented, Metal/Polymer + Additive, Cemented, OQI - Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3350, 888.3353, 888.3358 |
| Review panels | Orthopedic |
| Registered establishments | LYNX Medical Pennsylvania |
| Establishment registrations | 2528981 |
| FEI numbers | 2528981 |
| Establishment operations | Contract Sterilizer |
| 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