Data / Medical devices / Syringe, Piston / India
FDA-registered makers of Syringe, Piston in India: 6 establishments
6 establishments in India are registered with the FDA to make Syringe, Piston (product code FMF). 4 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
- Syringe, Piston
- Product code
- FMF
- Country
- India
Makers of Syringe, Piston in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hindustan Syringes & Medical Devices Ltd. | Faridabad Haryana, India | Manufacturer | 1 | January 26, 1995 | 0 | 0 | 0 | api.fda.gov |
| Lifelong Meditech Private Limited | Gurugram Haryana, India | Contract manufacturer, Exporter to the US, Manufacturer | 1 | July 18, 2023 | 0 | 0 | 0 | api.fda.gov |
| SMB Corporation Of India | Valsad Gujarat, India | Manufacturer | 1 | January 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| SPM Medicare Pvt, Ltd. | NOIDA Uttar Pradesh, India | Manufacturer | 1 | March 6, 2024 | 0 | 0 | 0 | api.fda.gov |
| Haselmeier India Private Limited | Bangalore Karnataka, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solco Biomedical Company India Private Limited | KADI Gujarat, 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.