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NovaPro Fill 21315-121

by Nanova Biomaterials Inc

NovaPro Fill 21315-121 is a Class II device made by Nanova Biomaterials Inc, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00816537020257), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816537020257 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  • Withdrawn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 Fill
Generic name
Dental composite resin
Model / Ref / Catalog
21315-121
Primary DI / UDI-DI
00816537020257
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

Similar devices in this category

Other devices filed under Dental composite resin.

Other devices from Nanova Biomaterials Inc

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Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)