Data / Medical devices / Gauze / Sponge,Nonresorbable For External Use / India
FDA-registered makers of Gauze / Sponge,Nonresorbable For External Use in India: 9 establishments
9 establishments in India are registered with the FDA to make Gauze / Sponge,Nonresorbable For External Use (product code NAB). 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
- Gauze / Sponge,Nonresorbable For External Use
- Product code
- NAB
- Country
- India
Makers of Gauze / Sponge,Nonresorbable For External Use in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aegis Lifesciences Private Limited | Ahmedabad Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Datt Mediproducts Private Limited | SOHNA Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DR. Sabharwal's Wound Care | BAROTIWALA Himachal Pradesh, India | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eon Curemed Private Limited | SURAT, Gujarat, India | Complaint file establishment, Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eon Meditech Pvt. Ltd. | Surat Gujarat, India | Complaint file establishment, Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| G Surgiwear Limited | Shahjahanpur Uttar Pradesh, 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 | |
| Narang Medical, Ltd. | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Premier Enterprises | Virudhunagar Tamil Nadu, 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.