FDA applicant

Lifestream Technologies, Inc.

Post Falls, ID3 decisions1999–20040 recalls

FDA records 3 decisions for Lifestream Technologies, Inc. (Post Falls, ID) from 1999 to 2004: 3 510(k) clearances. Most are in product codes CHH (Enzymatic Esterase--Oxidase, Cholesterol) and NFX (Test, Cholesterol, Total, Over The Counter). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Lifestream Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifestream Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lifestream Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Lifestream”

FDA records each applicant name separately; these may or may not be the same firm.

Lifestream Int'L, Inc. 23 Lifestream Diagnostics, Inc. 1 Lifestream Purfication Systems, LLC 1

Lifestream Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lifestream”