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Concorde Lift 1978-09-021C

by Medos International Sàrl

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

2 closed

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10705034531601 UDI-DI Date9 Mar 2018ListedStatusListed GUDID: not in commercial distribution

Recalls

2 recalls · FDA

    • Terminated Z-1225-2019 FDA Class II initiated 8 Apr 2019

    A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

    • Terminated Z-0848-2018 FDA Class II initiated 26 Jul 2017

    Potential for Intra-operative breakage of driver tips

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Concorde Lift
Generic Name
Metallic spinal interbody fusion cage
Model / Ref / Catalog
1978-09-021C, 197809021C
Primary DI / UDI-DI
10705034531601
510(k) Number
FDA Product Code
MAX
GMDN Term
Metallic spinal interbody fusion cage
Device Class
Class II
Regulation Number
888.3080
GUDID distribution status
Not in Commercial Distribution

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No