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Inbone 220225412E

by Wright Medical Technology, Inc.

Inbone 220225412E is a Class II device made by Wright Medical Technology, Inc., listed in FDA GUDID since 1 Oct 2015 (UDI-DI 00840420125255), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840420125255 UDI-DI Date1 Oct 2015ListedStatusListed 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  • Withdrawn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
Inbone
Generic name
Fixed-bearing total ankle prosthesis
Model / Ref / Catalog
220225412E
Primary DI / UDI-DI
00840420125255
FDA product code
HSN
GMDN term
Fixed-bearing total ankle prosthesis
Device class
Class II
Regulation number
888.3110
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Height — 12 Millimeter

Related devices

Category: Fixed-bearing total ankle prosthesis

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties

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