FDA applicant
Life Sciences Manufacturing, Inc.
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
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.
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.
See the 510(k) Report