FDA applicant

Paladin Biomedical Corporation

Weston, MA1 decision2008–20080 recalls

FDA records 1 decision for Paladin Biomedical Corporation (Weston, MA) in 2008: 1 510(k) clearance. All are in product code LGZ (Warmer, Thermal, Infusion Fluid). 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, general hospital panel, where it files most

How often FDA has decided Paladin Biomedical Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Paladin Biomedical Corporation by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Paladin Biomedical Corporation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Paladin”

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

Paladin Medical, Inc. 14

Paladin Biomedical Corporation

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paladin”