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Gid 700

by The Gid Group, Inc.

510(k) K120902

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

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 NumberK120902 Date15 Aug 2012ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0823-2018 FDA Class II initiated 8 Aug 2017

    Presence of bacterial endotoxins levels above the acceptable limit

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  • Withdrawn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
MUU
Device Class
Class II
Regulation
21 CFR Part 878.5040
Advisory Committee
General, Plastic Surgery
FDA Decision
SESE Substantially Equivalent