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Tecnofar SpA

Country not established

Tecnofar SpA is a medical device manufacturer, with 21 devices listed in FDA GUDID (FDA Class I) as of 13 Nov 2026.

Devices
21

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 21
Device classes
  • FDA Class I 21
Identifiers
  • DUNS 428682363

What Tecnofar SpA makes

Tecnofar Spa manufactures single-use dental syringe needles designed for local anesthesia delivery in dental procedures. Their portfolio includes branded devices such as ORABLOC, SUPPRA JECT, SIRIO, and FAIRFAX DENTAL, which are intended for use in oral healthcare settings.

These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue21

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Company details

DUNS number
428682363
Phone
+39 0342684115

Frequently asked questions

How many devices does TECNOFAR SPA have in the registry?

The registry currently lists 21 devices for TECNOFAR SPA. Devices recorded under merged duplicate company entries are counted once.

Which registries list TECNOFAR SPA's devices?

Among its 21 most recently registered devices, TECNOFAR SPA has devices listed in FDA GUDID (21 devices).

What risk classes do TECNOFAR SPA's devices fall under?

Among its 21 most recently registered devices, the classes recorded for TECNOFAR SPA's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from TECNOFAR SPA in the registry?

The most recently registered devices listed for TECNOFAR SPA include EFFITEC 30G EXTRA SHORT, EFFITEC 30G SHORT, EFFITEC 27G SHORT and Orabloc Needle twenty7L.

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