Establishment registration
PREMIER DENTAL PRODUCTS CO.
FDA establishment registration 2511556 · PLYMOUTH MEETING, US
Key facts
| Registration number | 2511556 |
|---|---|
| Establishment name | PREMIER DENTAL PRODUCTS CO. |
| Owner/operator | Premier Dental Products Company |
| Owner/operator number | 2511556 |
| FEI number | 2511556 |
| Address | 1710 Romano Dr |
| City | PLYMOUTH MEETING |
| State | PA |
| Country | US |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BTO, DYH, DZA, DZN, DZP, EBC, EBF, EFC, EFK, EFN, EGN, EHJ, EHK, EHM, EHY, EID, EIG, EIK, EIL, EIR, EIS, EIX, EIY, EJB, EJG, EJP, EJQ, EJR, EJY, EJZ and 71 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- None 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