Skip to content

Bioblend® Anteriors 110 L R

by Dentsply International

Listed FDA GUDID listing, not in commercial distribution

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 NumberD00116346L110R0 UDI-DI Date10 Oct 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Bioblend® Anteriors
Generic Name
Resin artificial teeth
Model / Ref / Catalog
110 L R, 16346
Primary DI / UDI-DI
D00116346L110R0
FDA Product Code
ELM
GMDN Term
Resin artificial teeth
Device Class
Class II
Regulation Number
872.3590
GUDID distribution status
Not in Commercial Distribution

Other devices from Dentsply International

See all devices from Dentsply International →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • 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
  • Expiration Date: No
  • Manufacturing Date: No