Skip to content

Medyssey Spinal System - Deformity LPH0905

by Medyssey Co., Ltd. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08806364639168 UDI-DIDate18 Aug 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Medyssey Spinal System - Deformity
Generic Name
Bone-screw internal spinal fixation system hook
Model / Reference
LPH0905
Primary DI / UDI-DI
08806364639168
FDA Product Code
KWP, MNH, MNI
GMDN Term
Bone-screw internal spinal fixation system hook
Device Class
Class II
Regulation Number
888.3050, 888.3070
GUDID distribution status
In Commercial Distribution
Sterilization 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

  • Single Use
  • Implantable
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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