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Ticonium 62174K25

by Cmp Industries LLC

Ticonium 62174K25 is a Class II device made by Cmp Industries LLC, listed in FDA GUDID since 8 Nov 2016 (UDI-DI M48262174K250), 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 NumberM48262174K250 UDI-DI Date8 Nov 2016ListedStatusListed 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  • Withdrawn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
Ticonium
Generic name
Dental casting non-noble alloy
Model / reference
62174K25
Primary DI / UDI-DI
M48262174K250
FDA product code
EJH
GMDN term
Dental casting non-noble alloy
Device class
Class II
Regulation number
872.3710
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental casting non-noble alloy

Similar devices in this category

Other devices filed under Dental casting non-noble alloy.

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See all devices from Cmp Industries LLC →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)