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Nanova Biomaterials Inc

United Statesfrom the FDA registration address FDA establishment FEI 3011430871

Nanova Biomaterials Inc is a medical device manufacturer, with 184 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 12 Nov 2026.

Devices
184
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 176
  • FDA 510(k) 8

A device listed in two registries counts in both.

Device classes
  • FDA Class II 184
Identifiers
  • FDA FEI 3011430871

What Nanova Biomaterials Inc makes

Nanova Biomaterials Inc manufactures dental composite resins, dental coating tooth-desensitizing products, fluoride gels, bioabsorbable orthopaedic bone screws, dental unfilled resin sealants/coatings, and synthetic polymer non-bioabsorbable ligation clips.

AI-generated from registry data, 6 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue184

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Company details

FDA FEI number
3011430871
Address
3806 Mojave Ct, Columbia, MO, 65202

Frequently asked questions

How many devices does NANOVA BIOMATERIALS INC have in the registry?

The registry currently lists 184 devices for NANOVA BIOMATERIALS INC. Devices recorded under merged duplicate company entries are counted once.

Which registries list NANOVA BIOMATERIALS INC's devices?

Among its 50 most recently registered devices, NANOVA BIOMATERIALS INC has devices listed in FDA GUDID (50 devices).

What risk classes do NANOVA BIOMATERIALS INC's devices fall under?

Among its 50 most recently registered devices, the classes recorded for NANOVA BIOMATERIALS INC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from NANOVA BIOMATERIALS INC in the registry?

The most recently registered devices listed for NANOVA BIOMATERIALS INC include FiberFIX 160129-1, FiberFIX 160135-1, FiberFIX 160145-1 and FiberFIX 190145-1.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.