Data / Medical devices / Chair And Table, Medical / India
FDA-registered makers of Chair And Table, Medical in India: 12 establishments
12 establishments in India are registered with the FDA to make Chair And Table, Medical (product code KMN). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Chair And Table, Medical
- Product code
- KMN
- Country
- India
Makers of Chair And Table, Medical in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Apothecaries Sundries MFG Pvt Ltd | GURUGRAM Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Balaji Surgical | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carevel Medical Systems Private Limited | GHAZIABAD Uttar Pradesh, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Endonest Medical Systems LLP | PALGHAR Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Galaxy India | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| M/S Royal Safe Company KB | New Delhi, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mark Enterprises | Nashik Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marken Healthtech Limited | NASHIK Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Narang Medical, Ltd. | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paras Surgico Factory | Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| United Medi Equip Private Limited | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| United Surgical Industries | SAHIBABAD Uttar Pradesh, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.