Data / Medical devices / File, Pulp Canal, Endodontic / India
FDA-registered makers of File, Pulp Canal, Endodontic in India: 5 establishments
5 establishments in India are registered with the FDA to make File, Pulp Canal, Endodontic (product code EKS). 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
- File, Pulp Canal, Endodontic
- Product code
- EKS
- Country
- India
Makers of File, Pulp Canal, Endodontic in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| J C India | Rajkot Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mothers Medica Private Limited | Chennai Tamil Nadu, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orikam Healthcare India Private Limited | Gurgaon Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prevest Denpro Limited | Jammu Jammu and Kashmir, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reach Global India Pvt Ltd | Pune Maharashtra, 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.