Data / Medical devices / India / Hindustan Syringes & Medical Devices Ltd.
Hindustan Syringes & Medical Devices Ltd.: FDA-registered device maker in Faridabad Haryana, India, 3 510(k) clearances
Hindustan Syringes & Medical Devices Ltd. is registered with the FDA (registration 3015724078) in Faridabad Haryana, India. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 12, 2001. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015724078
- Address
- 99/25 Ballabgarh, Faridabad Haryana, India, 121004
- Owner or operator
- HINDUSTAN SYRINGES & MEDICAL DEVICES, LTD. (8040227)
- Roles
- Manufacturer
- First device listed
- January 13, 2008
- Registered through
- 2026
- Brand names listed
- DISPO VAN, UNOLOK, UNOLOK PLUS, VAKU-8
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FOZ | 2 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Manufacturer | accessdata.fda.gov |
| System, Blood Collection, Vacuum-Assisted, Manual | KST | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 12, 2001 | K000592 | UNOLOK PLUS INFUSION SET AND VAKU-8 PLUS BLOOD COLLECTION SET | FPA | Substantially Equivalent | Myco Medical Supplies, Inc. | accessdata.fda.gov |
| November 26, 1996 | K953252 | DISPOSABLE SCALP VEIN INFUSION SET | FOZ | Substantially Equivalent | Myco Medical Supplies, Inc. | accessdata.fda.gov |
| January 26, 1995 | K945225 | DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES | FMF | Substantially Equivalent | Myco Medical Supplies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- All makers of Set, Administration, Intravascular
- All makers of System, Blood Collection, Vacuum-Assisted, Manual
- All makers of Syringe, Piston
- All makers of Needle, Hypodermic, Single Lumen
Updated April 12, 2001. 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.