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A. Titan Instruments XT 113

by A.Titan Instruments

A. Titan Instruments XT 113 is a Class I device made by A.Titan Instruments, cleared under FDA 510(k) K060691 on 12 Jun 2006 and listed in FDA GUDID since 19 Jan 2023 (UDI-DI 00841685102067), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K060691

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841685102067 UDI-DI Date19 Jan 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK060691 Date12 Jun 2006DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K060691 decided 12 Jun 2006 Active
  • FDA GUDID UDI-DI 00841685102067 listed 19 Jan 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K060691
  2. Listed FDA GUDID 00841685102067

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
A. Titan Instruments
Generic name
Tooth extraction forceps
Model / reference
XT 113
Primary DI / UDI-DI
00841685102067
510(k) Number
FDA product code
EMG
GMDN term
Tooth extraction forceps
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Dry Heat Sterilization

Related devices

Category: Tooth extraction forceps

Cleared under the same submission (K060691)

and 8 more cleared under K060691

Other devices from A.Titan Instruments

See all devices from A.Titan Instruments →

Properties

  • Sterilise before use
  • Lot / batch number
Other properties (13, all answered No)