LZMClass I

Guard, Skin Graft

21 CFR 878.4014 / General, Plastic Surgery

LZM is the FDA product code for Guard, Skin Graft, a class I device type, regulated under 21 CFR 878.4014. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1994-09-30, and no recalls.

Classification record

Product code: LZM
Device name: Guard, Skin Graft
Regulation: 21 CFR 878.4014
Device class: Class I
Review panel: General, Plastic Surgery
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code LZM

By decision year

2 clearances under product code LZM with a decision year between 1989 and 1994, 1989 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code LZM by decision year
Year	Clearances
1989	1
1994	1

Applicants with the most clearances

Product code LZM

Applicants holding the most 510(k) clearances under product code LZM
Applicant	Clearances
Sorex Medical	1
Anholt Technologies Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LZM.

Recent clearances

Product code LZM

Recent recalls

Product code LZM

FDA records show no recalls under product code LZM.

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)