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DIOnavi-C&B Z 3DCNBF-1000A4

by DIO Corporation

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800049401484 UDI-DI Date1 Dec 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
DIOnavi-C&B Z
Generic Name
Dental prosthesis veneer resin
Model / Reference
3DCNBF-1000A4
Primary DI / UDI-DI
08800049401484
FDA Product Code
NDP
GMDN Term
Dental prosthesis veneer resin
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental prosthesis veneer resin

Other devices from DIO Corporation

See all devices from DIO Corporation →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No