Data / Medical devices / Blade, Scalpel / India
FDA-registered makers of Blade, Scalpel in India: 14 establishments
14 establishments in India are registered with the FDA to make Blade, Scalpel (product code GES). 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
- Blade, Scalpel
- Product code
- GES
- Country
- India
Makers of Blade, Scalpel 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 | |
| Aditya Dispomed Products Pvt Ltd. | IMT Manesar Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Auxein medical Private limited | Sonipat Haryana, India | 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 | |
| HMD Healthcare India Pvt. Ltd. | Faridabad Haryana, India | Manufacturer | 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 | |
| Jai Surgicals Ltd. | ALWAR Rajasthan, India | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meditec Devices | Vasai(E), Thane, Maharashtra, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Narang Medical, Ltd. | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paramount Surgimed Ltd. | BHIWADI Rajasthan, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Razormed Inc. | GURGAON Haryana, India | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ribbel International Ltd. | SONEPAT Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surgimed Devices | AHMEDABAD Gujarat, 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.