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Ankle Compression Nailing System 1

by Orthofix, Inc. 49 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number18033509858352 UDI-DI Date1 Sep 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ankle Compression Nailing System
Generic Name
Arthrodesis intramedullary nail, non-distracting
Model / Ref / Catalog
1, 99-T770250
Primary DI / UDI-DI
18033509858352
FDA Product Code
JDS, HSB
GMDN Term
Arthrodesis intramedullary nail, non-distracting
Device Class
Class II
Regulation Number
888.3030, 888.3020
GUDID distribution status
In Commercial Distribution
Size
Length — 250 Millimeter
Outer Diameter — 10 Millimeter

Related devices

Category: Arthrodesis intramedullary nail, non-distracting

Other devices from Orthofix, Inc.

See all devices from Orthofix, Inc. →

Properties

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

Other properties (6)

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