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Consensus MBK System 2162-0-1220

by Shalby Advanced Technologies, Inc.

Consensus MBK System 2162-0-1220 is a Class II device made by Shalby Advanced Technologies, Inc., listed in FDA GUDID since 28 Jan 2022 (UDI-DI 00840286817776), 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 Number00840286817776 UDI-DI Date28 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  • Withdrawn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 MBK System
Generic name
Posterior-stabilized total knee prosthesis
Model / Ref / Catalog
2162-0-1220
Primary DI / UDI-DI
00840286817776
FDA product code
JWH
GMDN term
Posterior-stabilized total knee prosthesis
Device class
Class II
Regulation number
888.3560
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JWH (PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER).

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)