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Tri B

by Tri Dental Implants Int. AG 80 variants

Tri B (TO41M06) is a Class II device made by Tri Dental Implants Int. AG, listed in FDA GUDID since 30 Jan 2019 (UDI-DI 07640149880557), 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 Number07640149880557 UDI-DI Date30 Jan 2019ListedStatusListed 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  • Withdrawn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
Tri
Generic name
Dental implant system
Model / Ref / Catalog
B, TO41M06
Primary DI / UDI-DI
07640149880557
FDA product code
DZE
GMDN term
Dental implant system
Device class
Class II
Regulation number
872.3640
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Dental implant system

Similar devices in this category

Other devices filed under Dental implant system.

Other devices from Tri Dental Implants Int. AG

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)