510(k) Report

FDA applicant

Life Sciences Manufacturing, Inc.

West Lebanon, NH12 decisions1979–19910 recalls

FDA records 12 decisions for Life Sciences Manufacturing, Inc. (West Lebanon, NH) from 1979 to 1991: 12 510(k) clearances. Most are in product codes DXG (Computer, Diagnostic, Pre-Programmed…) and DSB (Plethysmograph, Impedance). 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, cardiovascular panel, where it files most

How often FDA has decided Life Sciences Manufacturing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Life Sciences Manufacturing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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