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Microlux Dl

by Addent, Inc.

510(k) K041614

Microlux Dl is a Class I device made by Addent, Inc., cleared under FDA 510(k) K041614 on 4 Apr 2005, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK041614 Date4 Apr 2005ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
EAZ
Device class
Class I
Regulation
21 CFR Part 872.4630
Advisory committee
Dental
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code EAZ (Light, Operating, Dental).

Other devices from Addent, Inc.

  • AdDent Compex HD

    Class I

  • AdDent OraBlu

    Class II

  • AdDent Microlux

    Class II

  • AdDent Calset

    Class I

See all devices from Addent, Inc. →