# Probo Medical Ltd (foreign exporter, Gloucester Gloucestershire, GB): 19 new FDA device listings, incl. endoscopic video imaging system/component, gastroenterology-urology

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Probo Medical Ltd |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Gloucester Gloucestershire, GB |
| New listings | 19 |
| Devices | Endoscopic Video Imaging System/Component, Gastroenterology-Urology; Transducer, Ultrasonic, Diagnostic; System, Imaging, Pulsed Echo, Ultrasonic; System, Imaging, Pulsed Doppler, Ultrasonic; Injector And Syringe, Angiographic; Full Field Digital, System, X-Ray, Mammographic; System, X-Ray, Tomography, Computed; Bronchoscope (Flexible Or Rigid); Endoscope, Accessories, Narrow Band Spectrum; System, Tomography, Computed, Emission |
| Product codes | FET, ITX, IYO, IYN, DXT, MUE, JAK, EOQ, NWB, KPS, FAJ, OXO, JAA, OWB |
| Device classes | Class II |
| Medical specialties | Gastroenterology, Urology, Radiology, Cardiovascular, Ear, Nose, Throat |
| Brand names | Olympus Camera Head; GE Voluson S10; Medrad Spectris Injector; GE Senographe Essential; Toshiba Aqulion; Olympus Processor; Siemens Biograph Horizon; GE Logiq E10 |
| First new listing | 2026-05-06 |
| Latest new listing | 2026-09-22 |
| FDA registration number | 3010398867 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- Listed in the last 45 days.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.