# Can Technomed Trading Ltd. (foreign exporter, Richmond British Columbia, CA): 40 new FDA device listings, incl. system, tomography, computed, emission

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Can Technomed Trading Ltd. |
| Owner / operator | Can Technomed Trading LTD. |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Richmond British Columbia, CA |
| New listings | 40 |
| Devices | System, Tomography, Computed, Emission; System, X-Ray, Tomography, Computed; System, X-Ray, Mammographic; Injector And Syringe, Angiographic; Densitometer, Bone; System, X-Ray, Tomographic; System, X-Ray, Stationary; Solid State X-Ray Imager (Flat Panel/Digital Imager); System, Nuclear Magnetic Resonance Imaging; System, Nuclear Magnetic Resonance Spectroscopic |
| Product codes | KPS, JAK, IZH, DXT, KGI, IZF, KPR, MQB, LNH, LNI, HQE, HQC, JAA, OXO, OWB |
| Device classes | Class II |
| Medical specialties | Radiology, Cardiovascular, Ophthalmic |
| Brand names | Siemens Symbia T6 Spare Parts; SIEMENS MAMMOMAT 3000; Spare Part- Siemens Definition AS Gantry; Siemens CT Scan Definition AS; GE CT Scan Revolution EVO; CT scan Injector; GE BMD Lunar Series; GE Digital Radiology Discovery XR650 |
| First new listing | 2026-05-06 |
| Latest new listing | 2026-10-15 |
| FDA registration number | 3015276088 |
| Registration expires | 2027-12-31 |

## 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.