FDA applicant

Althin Biopharm, Inc.

Laval, Quebec, CA1 decision1999–19990 recalls

FDA records 1 decision for Althin Biopharm, Inc. (Laval, Quebec, CA) in 1999: 1 510(k) clearance. All are in product code KPO (Dialysate Concentrate For Hemodialysis (Liquid…). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Althin Biopharm, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Althin Biopharm, 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 “Althin”

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

Althin Medical AB an Affiliate of Baxter Intl 27 Althin Medical AB 7

Althin Biopharm, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Althin”