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Flow-FX2 71-0050

by Etex Corp.

Flow-FX2 71-0050 (71-0025) is a Class II device made by Etex Corp., listed in FDA GUDID since 23 Jan 2019 (UDI-DI 00889024499706), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024499706 UDI-DI Date23 Jan 2019ListedStatusListed 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  • Withdrawn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
Flow-FX2
Generic name
Synthetic bone graft
Model / Ref / Catalog
71-0050, 71-0025
Primary DI / UDI-DI
00889024499706
FDA product code
MQV
GMDN term
Synthetic bone graft
Device class
Class II
Regulation number
888.3045
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 5 Milliliter

Related devices

Category: Synthetic bone graft

Similar devices in this category

Other devices filed under Synthetic bone graft.

Other devices from Etex Corp.

See all devices from Etex Corp. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (8, all answered No)