Data / Medical devices / United States / Healthline Trading LLC.
Healthline Trading LLC.: FDA-registered device maker in Brooklyn, NY, United States, 1 510(k) clearance
Healthline Trading LLC. is registered with the FDA (registration 3005858417) in Brooklyn, NY, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 18, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005858417
- Address
- 4201 ave H, Brooklyn, NY, United States, 11210
- Owner or operator
- HEALTHLINE TRADING LLC. (10037538)
- Roles
- Manufacturer
- First device listed
- September 12, 2012
- Registered through
- 2026
- Brand names listed
- BEDDING, DISPOSABLE, MEDICAL, BEDDING,DISPOSABLE,MEDICAL, GARMENT, PROTECTIVE, FOR INCONTINENCE, GARMENT,PROTECTIVE,FOR INCONTINENCE, Wheelchair, mechanical
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bedding, Disposable, Medical | KME | 1 | Manufacturer | accessdata.fda.gov |
| Garment, Protective, For Incontinence | EYQ | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 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 18, 2012 | K112816 | ZHENJIANG ASURE MECHANICAL WHEELCHAIR | IOR | Substantially Equivalent | Zhenjiang Assure Medical Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Bedding, Disposable, Medical
- All makers of Wheelchair, Mechanical
- All makers of Garment, Protective, For Incontinence
Updated April 18, 2012. 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.