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Kentron 739925

by Kentron Health Care, Inc.

Kentron 739925 is a Class II device made by Kentron Health Care, Inc., cleared under FDA 510(k) K140228 on 18 Dec 2014 and listed in FDA GUDID since 27 May 2026 (UDI-DI 00810003750402), 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) K140228

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 Number00810003750402 UDI-DI Date27 May 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK140228 Date18 Dec 2014DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K140228 decided 18 Dec 2014 Active
  • FDA GUDID UDI-DI 00810003750402 listed 27 May 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K140228
  2. Listed FDA GUDID 00810003750402

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Kentron
Generic name
Basic endotracheal tube, single-use
Model / reference
739925
Primary DI / UDI-DI
00810003750402
510(k) Number
FDA product code
BTR
GMDN term
Basic endotracheal tube, single-use
Device class
Class II
Regulation number
868.5730
GUDID distribution status
In Commercial Distribution

Other devices from Kentron Health Care, Inc.

  • Kentron 739920

    Class II
  • Kentron 739930

    Class II
  • Kentron 739935

    Class II
  • Kentron 739945

    Class II

See all devices from Kentron Health Care, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)