Diros Technology, Inc.
Country not established
Diros Technology, Inc. is a medical device manufacturer, with 435 devices listed in FDA GUDID, FDA 510(k) and EUDAMED (FDA Class II; EU Class IIb) as of 12 Nov 2026.
- Devices
- 435
Registry facts
- Registries
- FDA GUDID 423
- FDA 510(k) 8
- EUDAMED 6
- Device classes
- FDA Class II 431
- EU Class IIb 4
- Top EMDN categories
- Sites and related companies
- Diros Technology, Inc. Canada
- Identifiers
- DUNS 202738675
Catalogue
Search and filter all 435 devicesShowing 1-50 of 435
Company details
- DUNS number
- 202738675
- RBAKER@DIROSTECH.COM
- Phone
- 9054153440
Sites
- Diros Technology, Inc. CAFEI 3003630373 4 devices
Frequently asked questions
How many devices does Diros Technology, Inc. have in the registry?
The registry currently lists 435 devices for Diros Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diros Technology, Inc.'s devices?
Among its 50 most recently registered devices, Diros Technology, Inc. has devices listed in EUDAMED (5 devices) and FDA GUDID (46 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Diros Technology, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Diros Technology, Inc.'s devices are Class IIb and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diros Technology, Inc. in the registry?
The most recently registered devices listed for Diros Technology, Inc. include OWL GD-Pad Patient Return Electrode (Split Type, Non-Corded), OWL GD-Pad Patient Return Electrode (Split Type, Corded), OWL GD-Pad Patient Return Electrode (Corded) and OWL GD-Pad Patient Return Electrode (Non-Corded).