Skip to content

CMORE® System, Rod Pusher 45-310

by Icotec GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07640172552971 UDI-DIDate24 Nov 2025ListedStatusListed 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  • Withdrawn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
CMORE® System, Rod Pusher
Generic Name
Orthopaedic rod reducer
Model / Ref / Catalog
45-310
Primary DI / UDI-DI
07640172552971
FDA Product Code
OLO, NKG
GMDN Term
Orthopaedic rod reducer
Device Class
Class II
Regulation Number
882.4560, 888.3075
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Icotec

See all devices from Icotec →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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