FDA device listing
Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie) 36 French,Endolumik Fluorescence Guided Gastric…
FDA device listing 1226521414 · PADCO Holding Company, LLC dba DEM Medical dba Virtec Medica
Key facts
| Proprietary names | Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie) 36 French,Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie) 40 French |
|---|---|
| Owner/operator | PADCO Holding Company, LLC dba DEM Medical dba Virtec Medica |
| Owner/operator number | 10090436 |
| Product codes | KNT |
| Device names | KNT - Tubes, Gastrointestinal (And Accessories) |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.5980 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | PADCO HOLDING COMPANY, LLC |
| Establishment registrations | 3030708724 |
| FEI numbers | 3030708724 |
| Establishment operations | Contract Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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