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Viora Ltd

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Viora Ltd is a medical device manufacturer, with 78 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class IIb and IIa) as of 13 Nov 2026.

Devices
78

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 57
  • EUDAMED 45
  • FDA 510(k) 11

A device listed in two registries counts in both.

Device classes
  • FDA Class II 60
  • EU Class IIb 8
  • FDA Class I 8
  • EU Class IIa 2
Top EMDN categories
Sites and related companies
Identifiers
  • DUNS 514612758

Catalogue78

Newest first, rows 1-50 of 78

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Rows 1-50 of 78

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Company details

DUNS number
514612758
Phone
8884151192

Sites1

Frequently asked questions

How many devices does VIORA LTD have in the registry?

The registry currently lists 78 devices for VIORA LTD. Devices recorded under merged duplicate company entries are counted once.

Which registries list VIORA LTD's devices?

Among its 50 most recently registered devices, VIORA LTD has devices listed in EUDAMED (32 devices) and FDA GUDID (40 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do VIORA LTD's devices fall under?

Among its 50 most recently registered devices, the classes recorded for VIORA LTD's devices are Class I, Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.

What are the newest devices from VIORA LTD in the registry?

The most recently registered devices listed for VIORA LTD include V-FC Tips 2 Units, 10 V-FR tips after sterilization, V-FORM Handpiece Full Set and V-VR Tip 12 Units.

Generated automatically from registry data and not verified by a human reviewer.