Skip to content

TrollFoil Red

by Directa AB 2 variants

TrollFoil Red (12000600) is a Class I device made by Directa AB, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 17310230000795), 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 Number17310230000795 UDI-DI Date6 Dec 2022ListedStatusListed 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  • Withdrawn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
TrollFoil
Generic name
Dental articulator
Model / Ref / Catalog
Red, 12000600
Primary DI / UDI-DI
17310230000795
FDA product code
EFH
GMDN term
Dental articulator
Device class
Class I
Regulation number
872.6140
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EFH (Paper, Articulation).

Other devices from Directa AB

See all devices from Directa AB →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)