Skip to content

3Shape Scan Bodies BCG

by 3Shape TRIOS A/S

3Shape Scan Bodies BCG is a Class I device made by 3Shape TRIOS A/S, listed in FDA GUDID since 21 May 2021 (UDI-DI 05902729751346), 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 Number05902729751346 UDI-DI Date21 May 2021ListedStatusListed 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  • Withdrawn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
3Shape Scan Bodies
Generic name
Dental milling system, CAD/CAM, laboratory
Model / reference
BCG
Primary DI / UDI-DI
05902729751346
FDA product code
NDP
GMDN term
Dental milling system, CAD/CAM, laboratory
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 6.0 Millimeter

Related devices

Category: Dental milling system, CAD/CAM, laboratory

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from 3Shape TRIOS A/S

  • 3Shape

    Class I

  • Trios Move Pro C4.2

    Class II

  • TRIOS Dx R1.1

    Class II

  • TRIOS Dx R1.2

    Class II

See all devices from 3Shape TRIOS A/S →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (9, all answered No)