FDA device listing
Chronoceptor™,MetaStep™ Displacement Device,MetaStep™ Positioning Screw,MetaStep™ Saw Template,MetaStep™ Stamp,MetaStep™…
FDA device listing 1939315402 · MERETE GMBH
Key facts
| Proprietary names | Chronoceptor™,MetaStep™ Displacement Device,MetaStep™ Positioning Screw,MetaStep™ Saw Template,MetaStep™ Stamp,MetaStep™ Steinmann Nail,OsteoBridge™ IKA Knee Arthrodesis Cement Protection Cap,OsteoBridge™ IKA Knee Arthrodesis Distance Holder,OsteoBridge™ IKA Knee Arthrodesis Torque Limiter,OsteoBridge™ Trocar,T-Handle,Various handles with ratchet,Wirefix Retractor |
|---|---|
| Owner/operator | MERETE GMBH |
| Owner/operator number | 9048847 |
| Product codes | LXH |
| Device names | LXH - Orthopedic Manual Surgical Instrument |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | MERETE GMBH |
| Establishment registrations | 3002949614 |
| FEI numbers | 3002949614 |
| Establishment operations | Specification Developer |
| 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