Data / Medical devices / Automated Radiological Image Processing Software / India
FDA-registered makers of Automated Radiological Image Processing Software in India: 7 establishments
7 establishments in India are registered with the FDA to make Automated Radiological Image Processing Software (product code QIH). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Automated Radiological Image Processing Software
- Product code
- QIH
- Country
- India
Makers of Automated Radiological Image Processing Software in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Qure.ai Technologies Private Limited | Mumbai Maharashtra, India | Manufacturer | 4 | August 16, 2024 | 0 | 0 | 0 | api.fda.gov |
| Philips Global Business Services LLP - Ultrasound Business Unit | Baner Pune Maharashtra, India | Specification developer | 2 | June 3, 2020 | 0 | 0 | 0 | api.fda.gov |
| Philips India Limited - Ultrasound Business Unit | Bengaluru Karnataka, India | Specification developer | 2 | June 3, 2020 | 0 | 0 | 0 | api.fda.gov |
| Philips India Limited - Radiology Informatics, Clinical Informatics, Patient Care Informatics Business Units | Bengaluru Karnataka, India | Specification developer | 1 | January 22, 2026 | 0 | 0 | 0 | api.fda.gov |
| WIPRO GE HEALTHCARE PRIVATE Ltd. | BANGALORE Karnataka, India | Specification developer | 1 | October 29, 2021 | 0 | 0 | 0 | api.fda.gov |
| Wipro Ge Medical Device Manufacturing Private Limited | Bangalore Karnataka, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wipro GE Healthcare Private Ltd. | Bangalore Karnataka, India | 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.