Data / Medical devices / System, Nuclear Magnetic Resonance Spectroscopic / India
FDA-registered makers of System, Nuclear Magnetic Resonance Spectroscopic in India: 5 establishments
5 establishments in India are registered with the FDA to make System, Nuclear Magnetic Resonance Spectroscopic (product code LNI). 0 have 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
- India
Makers of System, Nuclear Magnetic Resonance Spectroscopic in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Philips Global Business Services LLP | Pune Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips India Limited - Magnetic Resonance Business Unit | Bengaluru Karnataka, India | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Pvt. Ltd. | Bangalore, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wipro Ge Healthcare Private Ltd | WHITEFIELD, BANGALORE Karnataka, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wipro Ge Medical Device Manufacturing Private Limited | Bangalore Karnataka, India | Manufacturer | 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.