LPZUnclassified

Container, Frozen Donor Tissue Storage

Unknown

LPZ is the FDA product code for Container, Frozen Donor Tissue Storage. As of 2026-09-10, FDA records hold 6 510(k) clearances under this code, the most recent dated 2002-08-06, and no recalls.

Classification record

Product code: LPZ
Device name: Container, Frozen Donor Tissue Storage
Device class: Unclassified
Review panel: Unknown
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 6
Ingested recalls: 0

Clearances, product code LPZ

By decision year

6 clearances under product code LPZ with a decision year between 1986 and 2002, 1986 the highest year at 3.

Show the numbers

510(k) clearances under FDA product code LPZ by decision year
Year	Clearances
1986	3
1987	1
1994	1
2002	1

Applicants with the most clearances

Product code LPZ

Applicants holding the most 510(k) clearances under product code LPZ
Applicant	Clearances
Travenol Laboratories, S.A.	2
Ammerman Medical Enterprises, Inc.	1
Hydro-Med Products, Inc.	1
Janus Biomedical, Inc.	1
OriGen Biomedical, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code LPZ

Recent recalls

Product code LPZ

FDA records show no recalls under product code LPZ.

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)