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Lido(Tm) Workset

by Loredan Biomedical, Inc.

510(k) K880018

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 NumberK880018 Date26 Feb 1988ClearedStatusActive

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  • Withdrawn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
IKK
Device Class
Class II
Regulation
21 CFR Part 890.1925
Advisory Committee
Physical Medicine
FDA Decision
SESE Substantially Equivalent

Other devices from Loredan Biomedical, Inc.

  • Lido Lift

    Class II

  • Lido V-Tak

    Class II

  • Lido Linea

    Class II

  • Lido Active

    Class II

  • Lido(R) Linea

    Class I

  • Lido Back

    Class II

See all devices from Loredan Biomedical, Inc. →