Data / Medical devices / System, Imaging, Pulsed Doppler, Ultrasonic / Norway
FDA-registered makers of System, Imaging, Pulsed Doppler, Ultrasonic in Norway: 5 establishments
5 establishments in Norway are registered with the FDA to make System, Imaging, Pulsed Doppler, Ultrasonic (product code IYN). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- System, Imaging, Pulsed Doppler, Ultrasonic
- Product code
- IYN
- Country
- Norway
Makers of System, Imaging, Pulsed Doppler, Ultrasonic in Norway
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ge Vingmed Ultrasound A/S | HORTEN Vestfold, Norway | Manufacturer, Specification developer | 73 | September 2, 2026 | 0 | 2 | 0 | api.fda.gov |
| GE Vingmed Ultrasound AS | Oslo, Norway | Specification developer | 20 | July 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| GE Vingmed Ultrasound AS | Trondheim Trondelag, Norway | Specification developer | 20 | July 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| Medistim Asa | HORTEN Vestfold, Norway | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medistim Asa | Oslo, Norway | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.