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Mguide® Mg-STN7

by Dentsply Ih, Inc.

Mguide® Mg-STN7 is a Class I device made by Dentsply Ih, Inc., listed in FDA GUDID since 4 Apr 2024 (UDI-DI 07392532253201), 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 Number07392532253201 UDI-DI Date4 Apr 2024ListedStatusListed 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  • Withdrawn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
Mguide®
Generic name
Dental implantation drilling template, custom-made
Model / reference
MG-STN7
Primary DI / UDI-DI
07392532253201
FDA product code
NDP
GMDN term
Dental implantation drilling template, custom-made
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental implantation drilling template, custom-made

Other devices from Dentsply Ih, Inc.

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Properties

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