FDA applicant

Quantum Life Systems, Inc.

Great Meadows, NJ1 decision1986–19860 recalls

FDA records 1 decision for Quantum Life Systems, Inc. (Great Meadows, NJ) in 1986: 1 510(k) clearance. All are in product code DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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 Quantum Life Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Quantum Life Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Quantum Life Systems, 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 “Quantum”

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

Quantum Orthopedics, Inc. 6 Quantum Medical Imaging, LLC 5 Quantum Medical Systems, Inc. 5 Quantum Bioengineering, Ltd. 4 Quantum Co., Ltd. 3 Quantum Medical Concepts, LLC 2 Quantum Instruments Corp. 2 Quantum Surgical Sas 2 Quantum Devices, Inc. 2 Quantum Skincare, Inc. 1 Quantum Intl. 1 Quantum Medical Imaging Divison of Carestream 1

Quantum Life Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Quantum”