# Ads Dental System Inc. (repackager or relabeler, Ontario, CA): 7 new FDA device listings, incl. controller, foot, handpiece and cord

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Ads Dental System Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Ontario, CA, US |
| New listings | 7 |
| Devices | Controller, Foot, Handpiece And Cord; Locator, Root Apex; Handpiece, Direct Drive, Ac-Powered; Handpiece, Contra- And Right-Angle Attachment, Dental; Handpiece, Air-Powered, Dental; Scaler, Ultrasonic |
| Product codes | EBW, LQY, EKX, EGS, EFB, ELC |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Dental |
| Brand names | Dental Implant Unit (Model: Implant Air);Contra-angle handpiece: WP-1L, WJ-11L; DPEX V; Motopex; Contra-angle handpiece: WJ-45L, WJ-45TL;Dental Electric Motor:MT2,M2 Pro; AP-H; AP-H Plus; D8 LED |
| First new listing | 2026-07-28 |
| Latest new listing | 2026-07-28 |
| FDA registration number | 3015376465 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.