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FOUNDATION System LCL0711

by Corelink LLC

FOUNDATION System LCL0711 is a Class II device made by Corelink LLC, listed in FDA GUDID since 21 Jan 2016 (UDI-DI M725LCL0711), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM725LCL0711 UDI-DI Date21 Jan 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
FOUNDATION System
Generic name
Polymeric spinal interbody fusion cage
Model / Ref / Catalog
LCL0711
Description
FOUNDATION LARGE CERVICAL CAGE - 11 MM LORDOTIC
Primary DI / UDI-DI
M725LCL0711
FDA product code
MAX, ODP
GMDN term
Polymeric spinal interbody fusion cage
Device class
Class II
Regulation number
888.3080
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Height — 11 Millimeter
Angle — 7 degree

Related devices

Category: Polymeric spinal interbody fusion cage

Similar devices

Other devices filed under FDA product code MAX (Intervertebral fusion device with bone graft, lumbar).

Other devices from Corelink LLC

See all devices from Corelink LLC →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (10, all answered No)