# George Taub Products & Fusion Co., Inc. (repackager or relabeler, Jersey City, NJ): 2 new FDA device listings, incl. syringe, restorative and impression material

**Score:** 35/100

| Field | Value |
|---|---|
| Establishment | George Taub Products & Fusion Co., Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Jersey City, NJ, US |
| New listings | 2 |
| Devices | Syringe, Restorative And Impression Material; Needle, Dental |
| Product codes | EID, DZM |
| Device classes | Class I |
| Medical specialties | Dental |
| Brand names | Tips - Auto Mix; Tips - Applicator - Luer |
| First new listing | 2026-07-23 |
| Latest new listing | 2026-07-23 |
| FDA registration number | 2241860 |
| Registration expires | 2026-12-31 |

## Why this score
- 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.