Data / Medical devices / Instrument, Manual, Surgical, General Use / India
FDA-registered makers of Instrument, Manual, Surgical, General Use in India: 14 establishments
14 establishments in India are registered with the FDA to make Instrument, Manual, Surgical, General Use (product code MDM). 0 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
- Instrument, Manual, Surgical, General Use
- Product code
- MDM
- Country
- India
Makers of Instrument, Manual, Surgical, General Use in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aditya Dispomed Products Private Ltd. | Gurgaon Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Adroit Manufacturing Co. | Umbergaon Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Auxein medical Private limited | Sonipat Haryana, India | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Craftlink Medical Device Private Limited | Kolkata West Bengal, India | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Disposafe Health And Life Care Limited | Faridabad Haryana, India | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Greens Surgicals Private Limited | Vadodara Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gesco Healthcare Private Limited | CHENNAI, Tamil Nadu, India | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Harsoria Healthcare Pvt. Ltd. | Gurgoon Haryana, India | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heuer International (A division of GST Corporation Limited) | NOIDA Uttar Pradesh, India | Foreign private label distributor, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| International Instruments | Thrissur Kerala, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kashmir Surgical Works | AMBALA Haryana, India | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medimeas Instruments | Ambala Cantt Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sipcon Technologies Private Limited | Ambala Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Times Surgical Co. | Jaipur Rajasthan, 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.