Data / Medical devices / Container, Specimen, Non-Sterile / India
FDA-registered makers of Container, Specimen, Non-Sterile in India: 5 establishments
5 establishments in India are registered with the FDA to make Container, Specimen, Non-Sterile (product code NNI). 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
- Container, Specimen, Non-Sterile
- Product code
- NNI
- Country
- India
Makers of Container, Specimen, Non-Sterile in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Accumax Lab Devices Pvt Ltd | Gandhi nagar Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arck Technologies Innovations Pvt Ltd | Vasai Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hospital Equipment MFG. Co. | NOIDA Uttar Pradesh, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SVP Packing Industry Pvt Ltd | MUMBAI Maharashtra, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| United Poly Engineering Pvt. Ltd. | New Delhi, 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.