Data / Medical devices / India / Disposafe Health And Life Care Limited
Disposafe Health And Life Care Limited: FDA-registered device maker in Faridabad Haryana, India, 1 510(k) clearance
Disposafe Health And Life Care Limited is registered with the FDA (registration 3013683058) in Faridabad Haryana, India. It lists 11 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 14, 2018. Registered through 2026. FDA data exported November 3, 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
- 3013683058
- Address
- Plot No 1 and 2 Phase - Il Sector-59,Ballabhgarh, Faridabad Haryana, India, 121004
- Owner or operator
- Disposafe Health and Life Care Limited (10055185)
- Roles
- Contract manufacturer, Manufacturer, Specification developer
- First device listed
- June 16, 2017
- Registered through
- 2026
- Brand names listed
- Disposafe, Disposafe Dermal Curette
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bag, Urine Collecting, Ureterostomy | EXG | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Blade, Saw, General & Plastic Surgery, Surgical | GFA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Blade, Scalpel | GES | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Clamp, Umbilical | HFW | 2 | Manufacturer | accessdata.fda.gov |
| Curette | HTF | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Pump, Nebulizer, Electrically Powered | JPW | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Scalpel, One-Piece | GDX | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Stopcock, I.V. Set | FMG | 2 | Manufacturer | accessdata.fda.gov |
| Uroflowmeter | EXY | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| March 14, 2018 | K172266 | Dynarex Three-Way Stopcock | FMG | Substantially Equivalent | Dynarex Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Blade, Saw, General & Plastic Surgery, Surgical
- All makers of Curette
- All makers of Mask, Oxygen
- All makers of Uroflowmeter
- All makers of Stopcock, I.V. Set
- All makers of Instrument, Manual, Surgical, General Use
Updated March 14, 2018. 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.