Skip to content

Medyssey Spinal System - Deformity LAH403

by Medyssey Co., Ltd.

Medyssey Spinal System - Deformity LAH403 is a Class II device made by Medyssey Co., Ltd., listed in FDA GUDID since 18 Aug 2016 (UDI-DI 08806364640058), 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 Number08806364640058 UDI-DI Date18 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Medyssey Spinal System - Deformity
Generic name
Bone-screw internal spinal fixation system hook
Model / reference
LAH403
Primary DI / UDI-DI
08806364640058
FDA product code
MNI, MNH, KWP
GMDN term
Bone-screw internal spinal fixation system hook
Device class
Class II
Regulation number
888.3070, 888.3050
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone-screw internal spinal fixation system hook

Other devices from Medyssey Co., Ltd.

See all devices from Medyssey Co., Ltd. →

Properties

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