Data / Medical devices / Surgeon'S Gloves / India
FDA-registered makers of Surgeon'S Gloves in India: 11 establishments
11 establishments in India are registered with the FDA to make Surgeon'S Gloves (product code KGO). 9 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
- Surgeon'S Gloves
- Product code
- KGO
- Country
- India
Makers of Surgeon'S Gloves in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Primus Gloves Private Ltd. | Kakkanad, Cochin, Kerala, India | Manufacturer, Specification developer | 6 | June 9, 2017 | 0 | 0 | 0 | api.fda.gov |
| Ansell Sterile Solutions Pvt. Ltd | Erode Tamil Nadu, India | Contract manufacturer, Contract sterilizer, Manufacturer | 4 | August 3, 2021 | 0 | 0 | 0 | api.fda.gov |
| Kanam Latex Industries Pvt. Ltd. | NAGERCOIL Tamil Nadu, India | Contract manufacturer, Contract sterilizer, Manufacturer, Remanufacturer, Repackager or relabeler | 2 | March 14, 2003 | 0 | 0 | 0 | api.fda.gov |
| Amazing Rubber Products Pvt. Ltd | COCHIN Kerala, India | Exporter to the US, Manufacturer | 1 | March 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| Kanam Latex Industries Pvt. Ltd. | NAGERCOIL Tamil Nadu, India | Manufacturer | 1 | January 31, 1991 | 0 | 0 | 0 | api.fda.gov |
| Liberty Med Supplies Pvt Ltd | KOTTAYAM Kerala, India | Manufacturer | 1 | January 8, 2018 | 0 | 0 | 0 | api.fda.gov |
| MRK Healthcare PVT.LTD | PATAN Gujarat, India | Manufacturer | 1 | November 3, 2021 | 0 | 0 | 0 | api.fda.gov |
| Narang Medical, Ltd. | New Delhi, India | Manufacturer | 1 | January 31, 1991 | 0 | 0 | 0 | api.fda.gov |
| St.marys Rubbers Pvt Ltd | Kottayam Kerala, India | Manufacturer | 1 | December 11, 2015 | 0 | 0 | 0 | api.fda.gov |
| RFB Gloves | NOIDA Uttar Pradesh, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sanrea Healthcare Products Pvt Ltd | Palakkad Kerala, 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.