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Ardent 60007

by Whip-Mix Corp.

Ardent 60007 is a Class I device made by Whip-Mix Corp., listed in FDA GUDID since 5 Nov 2025 (UDI-DI D040600071), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD040600071 UDI-DI Date5 Nov 2025ListedStatusListed 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  • Withdrawn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
Ardent
Generic name
Dental articulation paper
Model / reference
60007
Primary DI / UDI-DI
D040600071
FDA product code
EFH
GMDN term
Dental articulation paper
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 Whip-Mix Corp.

See all devices from Whip-Mix Corp. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)