Establishment registration
JERSEY DENTAL SUPPLIES
FDA establishment registration 3012187973 · Lakewood, US
Key facts
| Registration number | 3012187973 |
|---|---|
| Establishment name | JERSEY DENTAL SUPPLIES |
| Owner/operator | Jersey Dental Supplies |
| Owner/operator number | 10050503 |
| FEI number | 3012187973 |
| Address | 1095 Towbin Ave |
| City | Lakewood |
| State | NJ |
| Country | US |
| Establishment types | Single-use device reprocessor |
| Registration valid through | 2026 |
| Product codes listed | BYG, DYH, DZE, DZN, DZS, EBC, EBD, EBF, EBG, EBH, EBI, EBZ, EFB, EHD, EHJ, EHL, EID, EIG, EIH, EJJ, EJK, EJR, EKQ, ELC, ELR, ELW, ELY, ELZ, EMA, EMB and 22 more |
| Device classes | 1, 2, 3, U |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database