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NovaPro Flow 63118-22

by Nanova Biomaterials Inc

NovaPro Flow 63118-22 is a Class II device made by Nanova Biomaterials Inc, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 30816537020210), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number30816537020210 UDI-DI Date16 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
NovaPro Flow
Generic name
Dental composite resin
Model / Ref / Catalog
63118-22
Primary DI / UDI-DI
30816537020210
FDA product code
EBF
GMDN term
Dental composite resin
Device class
Class II
Regulation number
872.3690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental composite resin

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Other devices filed under Dental composite resin.

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Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)