FDA device listing
ATTUNE REVISION TIBIAL SLEEVE SEPARATOR - DRIVER,TELIGEN,various prosthesis drivers
FDA device listing 1500585269 · DePuy Synthes, Inc.
Key facts
| Proprietary names | ATTUNE REVISION TIBIAL SLEEVE SEPARATOR - DRIVER,TELIGEN,various prosthesis drivers |
|---|---|
| Owner/operator | DePuy Synthes, Inc. |
| Owner/operator number | 1818910 |
| Product codes | HWR |
| Device names | HWR - Driver, Prosthesis |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | DEPUY INTL., LTD., DEPUY (IRELAND), Depuy Ireland UC, DEPUY ORTHOPAEDICS, DEPUY ORTHOPAEDICS, INC. |
| Establishment registrations | 1219655, 1818910, 8010379, 9616671, 3004464325, 3015516266 |
| FEI numbers | 1219655, 1818910, 1000199976, 3002854251, 3004464325, 3015516266 |
| Establishment operations | Manufacturer, Specification Developer, Repackager/Relabeler |
| 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