Data / Medical devices / India / Advanced Lifesciences Pvt. Ltd.
Advanced Lifesciences Pvt. Ltd.: FDA-registered device maker in New Delhi, India, 1 510(k) clearance
Advanced Lifesciences Pvt. Ltd. is registered with the FDA (registration 3007830707) in New Delhi, India. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 6, 2022. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007830707
- Address
- D-22 Okhla Industrial Area Phase-1, New Delhi, India, 110020
- Owner or operator
- Advanced LifeSciences Pvt. Ltd. (10058669)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- October 18, 2018
- Registered through
- 2027
- Brand names listed
- AD-Valve, ALSPL GUIDEWIRE, Cervical Dilator, Control Syringe, Glider, Guidewire, Hemostasis Valve, Inflation Device and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Catheter | KGZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | DTL | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Catheter, Intravascular, Diagnostic | DQO | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Clamp, Vascular | DXC | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Dilator, Cervical, Fixed Size | HDQ | 1 | Contract manufacturer | accessdata.fda.gov |
| Introducer, Catheter | DYB | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Syringe, Balloon Inflation | MAV | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wire, Guide, Catheter | DQX | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wire, Guide, Catheter, Exempt | PTL | 2 | 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 |
|---|---|---|---|---|---|---|
| October 6, 2022 | K213666 | NuCath Wedge Pressure Catheter | DQO | Substantially Equivalent | Pfm Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Intravascular, Diagnostic
- All makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- All makers of Wire, Guide, Catheter
- All makers of Introducer, Catheter
- All makers of Clamp, Vascular
- All makers of Accessories, Catheter
Updated October 6, 2022. 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.