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Everstick Post

by Stick Tech, Ltd.

510(k) K030820

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

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK030820 Date20 May 2003ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
ELR
FDA applicant
Stick Tech , Ltd.
Device Class
Class I
Regulation
21 CFR Part 872.3810
Advisory Committee
Dental
FDA Decision
SESE Substantially Equivalent

Other devices from Stick Tech, Ltd.

  • Eversticknet

    Class II

  • Stick Flow

    Class II

  • Everstick

    Class II

  • Everstick Ortho

    Class II

  • Stick Net

    Class II

  • Everstick a&O

    Class II

See all devices from Stick Tech, Ltd. →