FDA device listing
3Dimensions System & Accessories,Dimensions Access System,Genius 3D Mammography,Hologic 3D mammogram,SELENIA DIMENSIONS…
FDA device listing 1819363063 · HOLOGIC, INC.
Key facts
| Proprietary names | 3Dimensions System & Accessories,Dimensions Access System,Genius 3D Mammography,Hologic 3D mammogram,SELENIA DIMENSIONS 3D SYSTEM & ACCESSORIES |
|---|---|
| Owner/operator | HOLOGIC, INC. |
| Owner/operator number | 9007676 |
| Premarket submissions | P080003 |
| Product codes | OTE |
| Device names | OTE - Digital Breast Tomosynthesis |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.OTE |
| Review panels | Radiology |
| Registered establishments | HOLOGIC, INC. |
| Establishment registrations | 3005496266 |
| FEI numbers | 3005496266 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 10–99 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database