Data / Medical devices / System, Nuclear Magnetic Resonance Spectroscopic / United States
FDA-registered makers of System, Nuclear Magnetic Resonance Spectroscopic in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make System, Nuclear Magnetic Resonance Spectroscopic (product code LNI). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- System, Nuclear Magnetic Resonance Spectroscopic
- Product code
- LNI
- Country
- United States
Makers of System, Nuclear Magnetic Resonance Spectroscopic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ge Medical Systems, LLC | Waukesha, WI, United States | Specification developer | 1 | August 22, 2001 | 0 | 0 | 0 | api.fda.gov |
| Brainspec, Inc | Framingham, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Healthcare Coils | Aurora, OH, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Healthcare Manufacturing LLC | Florence, SC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Healthcare Manufacturing LLC | Florence, SC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HM Product Solutions, Ltd. | Hartland, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| IMRIS Imaging, Inc. | Chaska, MN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nova Medical, Inc | Wilmington, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Electrodynamics | Mayfield Village, OH, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.