Data / Medical devices / India / Lifelong Meditech Private Limited
Lifelong Meditech Private Limited: FDA-registered device maker in Gurugram Haryana, India, 1 510(k) clearance
Lifelong Meditech Private Limited is registered with the FDA (registration 3017770710) in Gurugram Haryana, India. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 18, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017770710
- Address
- Mustkil No. 136 Main Pataudi Road, Village - Patli Hazipur, Gurugram Haryana, India, 122506
- Owner or operator
- Lifelong Meditech Private Limited (10078369)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- July 27, 2021
- Registered through
- 2026
- Brand names listed
- DYNAREX CORP, Dynarex, Hypodermic Syringe for single use, Bulk-pack, Non-sterile, NU-HORIZON PRODUCTS, Needle, hypodermic, single lumen, SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX, LIFELONG, CLICKZIP, SHIELDPRO, SYRINGE, ANTISTICK, SYRINGE, IRRIGATING (NON DENTAL) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Contract manufacturer, Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| July 18, 2023 | K222925 | Hypodermic Syringes & Needle | FMF | Substantially Equivalent | Lifelong Meditech Private Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Syringe, Antistick
- All makers of Syringe, Irrigating (Non Dental)
Updated July 18, 2023. 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.