Skip to content

Inbone 100072

by Wright Medical Technology, Inc.

Ref 100072

Inbone 100072 is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-00840420195760) and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00840420195760), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00840420195760 Basic UDI-DI 00840420195760UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00840420195760 UDI-DI Date17 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00840420195760 registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 00840420195760 listed 17 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00840420195760
  2. Registered EUDAMED B-00840420195760

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Inbone
Generic name
Orthopaedic implant aiming/guiding block, reusable
Device name
Inbone™ Anterior Adjust. Plate
Model / Ref / Catalog
100072
Primary DI / UDI-DI
00840420195760
Basic UDI-DI
B-00840420195760
FDA product code
LXH
EMDN code
L0915 Spreaders and retractors for orthopaedic surgery, reusable
GMDN term
Orthopaedic implant aiming/guiding block, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implant aiming/guiding block, reusable

Similar devices in this category

Other devices filed under SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE.

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)