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Master-Dent 25-312

by Dentonics, Inc.

Master-Dent 25-312 is a Class I device made by Dentonics, Inc., listed in FDA GUDID since 31 Oct 2023 (UDI-DI 00816526022910), 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 Number00816526022910 UDI-DI Date31 Oct 2023ListedStatusListed 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  • Withdrawn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
Master-Dent
Generic name
Dental impression tray, single-use
Model / reference
25-312
Primary DI / UDI-DI
00816526022910
FDA product code
EHY
GMDN term
Dental impression tray, single-use
Device class
Class I
Regulation number
872.6880
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental impression tray, single-use

Other devices from Dentonics, Inc.

See all devices from Dentonics, Inc. →

Properties

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