Data / Medical devices / Exerciser, Non-Measuring / India
FDA-registered makers of Exerciser, Non-Measuring in India: 6 establishments
6 establishments in India are registered with the FDA to make Exerciser, Non-Measuring (product code ION). 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
- Exerciser, Non-Measuring
- Product code
- ION
- Country
- India
Makers of Exerciser, Non-Measuring in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Engineered Elastomer Solutions | KOCHI Kerala, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Garware Fulflex India Private Ltd (Formerly Garware Bestretch Ltd) | SATARA Maharashtra, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innovate Polimer Company | KOCHI Kerala, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| M/S. Ascent Meditech Limited | GOREGAON (E) Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Steeoniq Manufacturing Private Limited | Bengaluru Karnataka, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tynor Orthotics (P) Ltd. | Mohali Punjab, 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.