Data / Medical devices / Bedding, Disposable, Medical / India
FDA-registered makers of Bedding, Disposable, Medical in India: 10 establishments
10 establishments in India are registered with the FDA to make Bedding, Disposable, Medical (product code KME). 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
- Bedding, Disposable, Medical
- Product code
- KME
- Country
- India
Makers of Bedding, Disposable, Medical in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Am Nonwovens | Madurai Tamil Nadu, India | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amaryllis Healthcare Pvt. Ltd | Bangalore Karnataka, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| C K Hygiene Pvt Ltd | Hyderabad Telangana, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| G Surgiwear Limited | Shahjahanpur Uttar Pradesh, 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 | |
| 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 | |
| Theni Guru Krishna Textile Mills (P) Ltd. | Theni Tamil Nadu, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Texbond Nonwovens | Pondicherry Puducherry, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zen Linen International Private Limited. | Chennai 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.