Data / Medical devices / System, Nuclear Magnetic Resonance Imaging / India
FDA-registered makers of System, Nuclear Magnetic Resonance Imaging in India: 7 establishments
7 establishments in India are registered with the FDA to make System, Nuclear Magnetic Resonance Imaging (product code LNH). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- System, Nuclear Magnetic Resonance Imaging
- Product code
- LNH
- Country
- India
Makers of System, Nuclear Magnetic Resonance Imaging in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Philips India Limited - Magnetic Resonance Business Unit | Bengaluru Karnataka, India | Specification developer | 26 | February 23, 2026 | 0 | 0 | 0 | api.fda.gov |
| Wipro Ge Healthcare Private Ltd | WHITEFIELD, BANGALORE Karnataka, India | Manufacturer | 17 | February 4, 2015 | 0 | 0 | 0 | api.fda.gov |
| Philips Global Business Services LLP | Pune Maharashtra, India | Manufacturer | 5 | March 22, 2011 | 0 | 0 | 0 | api.fda.gov |
| WIPRO GE HEALTHCARE PRIVATE Ltd. | BANGALORE Karnataka, India | Specification developer | 1 | October 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Wipro Ge Medical Device Manufacturing Private Limited | Bangalore Karnataka, India | Manufacturer | 1 | March 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Wipro GE Healthcare Private Ltd. | Bangalore Karnataka, India | Manufacturer | 1 | October 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthcare Pvt. Ltd. | Bangalore, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.