FDA device listing
[Target] TCU0002 Bone Curette 3.0mm Bishop,[Target] TCU0003 Bone Curette 5.0mm Maximus,[Target] TCU0004 Bone Curette…
FDA device listing 2044917819 · Solendos., INC.
Key facts
| Proprietary names | [Target] TCU0002 Bone Curette 3.0mm Bishop,[Target] TCU0003 Bone Curette 5.0mm Maximus,[Target] TCU0004 Bone Curette 6.0mm Wang,[Target] TCU0005 Reverse Curette 3.0mm,[Target] TCU0006 Boomerang Curette 3.0mm |
|---|---|
| Owner/operator | Solendos., INC. |
| Owner/operator number | 10089428 |
| Product codes | FZS |
| Device names | FZS - Curette, Surgical, General Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | SOLENDOS., INC. |
| Establishment registrations | 3027262786 |
| FEI numbers | 3027262786 |
| Establishment operations | 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