FDA device listing
PTEYE PARATHYROID AUTOFLUORESCENCE DETECTION DEVICE
FDA device listing 1579428321 · Medtronic, Inc.
Key facts
| Proprietary names | PTEYE PARATHYROID AUTOFLUORESCENCE DETECTION DEVICE |
|---|---|
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| Premarket submissions | DEN170056 |
| Product codes | QDF |
| Device names | QDF - Parathyroid Autofluorescence Detection Device |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4550 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Medtronic Engineering and Innovation Center (MEIC), MEDTRONIC POWERED SURGICAL SOLUTIONS, MEDTRONIC XOMED, INC. |
| Establishment registrations | 1045254, 1625507, 3018094310 |
| FEI numbers | 1045254, 1625507, 3018094310 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 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