Inbone IB100033

by Wright Medical Technology, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00889797047876 UDI-DI	Date17 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Inbone
Generic name: Orthopaedic implant aiming/guiding block, reusable
Model / Ref / Catalog: IB100033

Primary DI / UDI-DI: 00889797047876
FDA product code: LXH
GMDN term: Orthopaedic implant aiming/guiding block, reusable

Device class: Class I
Regulation number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Other devices from Wright Medical Technology, Inc.

Invision

Class IIa
Ortholoc® 3Di

Class I
Ortholoc 3Di

Class IIa
Inbone®

Class I
Invision®

Class I
Ortholoc® 3Di Crosscheck®

Class I

See all devices from Wright Medical Technology, Inc. →

Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (10)

Supplied sterile: No
Single use: No
Implantable: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Serial number: No
Expiration date: No