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FAICO CMF System MICS-1.2-S-11.0-TI

by Faico Medical LLC GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840192705662 UDI-DIDate13 Sep 2020ListedStatusListed GUDID: not 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  • Withdrawn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
FAICO CMF System
Generic Name
Craniofacial bone screw, non-bioabsorbable
Model / Reference
MICS-1.2-S-11.0-TI
Primary DI / UDI-DI
00840192705662
FDA Product Code
DZL
GMDN Term
Craniofacial bone screw, non-bioabsorbable
Device Class
Class II
Regulation Number
872.4880
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Faico Medical LLC

Properties

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

Other properties (8)

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