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Consensus Hip System 1020-0-1851

by Shalby Advanced Technologies, Inc.

Consensus Hip System 1020-0-1851 is a Class II device made by Shalby Advanced Technologies, Inc., listed in FDA GUDID since 15 Jan 2022 (UDI-DI 00840286804097), 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 Number00840286804097 UDI-DI Date15 Jan 2022ListedStatusListed 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  • Withdrawn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
Consensus Hip System
Generic name
Bipolar femoral head outer component, hemiarthroplasty
Model / Ref / Catalog
1020-0-1851
Primary DI / UDI-DI
00840286804097
FDA product code
KWY
GMDN term
Bipolar femoral head outer component, hemiarthroplasty
Device class
Class II
Regulation number
888.3390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bipolar femoral head outer component, hemiarthroplasty

Similar devices in this category

Other devices filed under Bipolar femoral head outer component, hemiarthroplasty.

Other devices from Shalby Advanced Technologies, Inc.

See all devices from Shalby Advanced Technologies, Inc. →

Properties

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