Data / Medical devices / Pad, Menstrual, Unscented / India
FDA-registered makers of Pad, Menstrual, Unscented in India: 10 establishments
10 establishments in India are registered with the FDA to make Pad, Menstrual, Unscented (product code HHD). 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
- Pad, Menstrual, Unscented
- Product code
- HHD
- Country
- India
Makers of Pad, Menstrual, Unscented in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aakar Innovations Private Limited | Valsad Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dynamic Techno Medicals Private Limited | Coimbatore Tamil Nadu, India | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Endonest Medical Systems LLP | PALGHAR Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fibril Tex Pvt Ltd. | Amritsar Punjab, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lords Mark Industries Ltd. | Daman and Diu Dadra and Nagar Haveli, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pan Healthcare Private Limited | Biliyada Gujarat, India | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sekhani Industries Pvt Ltd | Ahmedabad Gujarat, India | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sparkle Eco Innovations Private Limited | SURAT Gujarat, India | Contract manufacturer, Foreign private label distributor, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solis Hygiene Pvt. Ltd. | Dhar Indore Madhya Pradesh, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Swara Baby Products Limited | Dhar Indore Madhya Pradesh, India | Contract 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.