MPKHumanitarian device exemption

Semi-Constrained Metal/Polymer Finger Joint Prosthesis

Unknown

MPK is the FDA product code for Semi-Constrained Metal/Polymer Finger Joint Prosthesis. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: MPK
Device name: Semi-Constrained Metal/Polymer Finger Joint Prosthesis
Device class: Humanitarian device exemption
Review panel: Unknown
Submission type: FDA code 6
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code MPK

FDA records hold no clearances under product code MPK.

Recent recalls

Product code MPK

Z-1567-2022Class IIAn incorrect sizing label was applied to the carton packaging.Wright Medical Technology, Inc. / initiated 2022-07-27 / 17 devices

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)