FDA device listing
AS2000 B2/3,AS2000 M4,S1,S10,S2,S20,S21L,S21R,S3,S35,S75,S900,S900KL,S900K…
FDA device listing 1463801583 · NAKANISHI INC.
Key facts
| Proprietary names | AS2000 B2/3,AS2000 M4,S1,S10,S2,S20,S21L,S21R,S3,S35,S75,S900,S900KL,S900K LAD,S900L,S900SL,S950,S950BL,S950KL,S950L,S950SL,S950WL,SONIC SCALER WITH FIBER OPTIC,V-U15,V-U20,V-U25,V-U30,V-U35 |
|---|---|
| Owner/operator | NAKANISHI INC. |
| Owner/operator number | 8030216 |
| Premarket submissions | K991021 |
| Product codes | ELC |
| Device names | ELC - Scaler, Ultrasonic |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.4850 |
| Review panels | Dental |
| Registered establishments | NAKANISHI INC., NSK AMERICA CORP. |
| Establishment registrations | 1422375, 9611253 |
| FEI numbers | 1000139790, 3002807687 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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