Skip to content

Tornillo De Titanio Hexagonal Interna® 30° INTTUH30

by Biotechnology Institute Sl

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 Number08435389811220 UDI-DI Date22 Oct 2015ListedStatusListed 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  • Withdrawn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
Tornillo De Titanio Hexagonal Interna® 30°
Generic Name
Dental implant suprastructure, permanent, preformed
Model / Reference
INTTUH30
Primary DI / UDI-DI
08435389811220
FDA Product Code
DZE
GMDN Term
Dental implant suprastructure, permanent, preformed
Device Class
Class II
Regulation Number
872.3640
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Length — 5.3 Millimeter
Outer Diameter — 1.8 Millimeter

Related devices

Category: Dental implant suprastructure, permanent, preformed

Other devices from Biotechnology Institute Sl

See all devices from Biotechnology Institute Sl →

Properties

  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No