Establishment registration
PULPDENT CORPORATION
FDA establishment registration 1215305 · Watertown, US
Key facts
| Registration number | 1215305 |
|---|---|
| Establishment name | PULPDENT CORPORATION |
| Owner/operator | PULPDENT CORPORATION |
| Owner/operator number | 1215305 |
| FEI number | 1215305 |
| Address | 80 Oakland St |
| City | Watertown |
| State | MA |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | DYH, DZM, DZN, EAX, EBC, EBD, EBF, EBG, EBH, EBL, EFH, EFK, EID, EIE, EIK, EIS, EJE, EJK, EJR, EJY, EKI, EKJ, EKL, EKQ, EKR, EKS, EMA, EMB, EMN, JDZ and 7 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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