FDA device listing
Ti-Max Z45,Z45L
FDA device listing 2003975377 · NAKANISHI INC.
Key facts
| Proprietary names | Ti-Max Z45,Z45L |
|---|---|
| Owner/operator | NAKANISHI INC. |
| Owner/operator number | 8030216 |
| Premarket submissions | K121901 |
| Product codes | EGS |
| Device names | EGS - Handpiece, Contra- And Right-Angle Attachment, Dental |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4200 |
| Review panels | Dental |
| Registered establishments | NAKANISHI INC., NSK AMERICA CORP. |
| Establishment registrations | 1422375, 9611253 |
| FEI numbers | 1000139790, 3002807687 |
| Establishment operations | Complaint File Establishment, Repackager/Relabeler, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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