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Guide Taper Drill GTD4113

by Surgident

Guide Taper Drill GTD4113 is a Class I device made by Surgident, listed in FDA GUDID since 17 Feb 2023 (UDI-DI 08800041044856), 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 Number08800041044856 UDI-DI Date17 Feb 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  • Withdrawn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
Guide Taper Drill
Generic name
Fixture/appliance dental drill bit, reusable
Model / reference
GTD4113
Primary DI / UDI-DI
08800041044856
FDA product code
NDP
GMDN term
Fixture/appliance dental drill bit, reusable
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Fixture/appliance dental drill bit, reusable

Similar devices in this category

Other devices filed under Fixture/appliance dental drill bit, reusable.

Other devices from Surgident

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)