Data / Medical devices / China / HL Corp. (shenzhen)
HL Corp. (shenzhen): FDA-registered device maker in BAOAN DISTRICT, SHENZHEN Guangdong, China, 1 510(k) clearance
HL Corp. (shenzhen) is registered with the FDA (registration 3004496806) in BAOAN DISTRICT, SHENZHEN Guangdong, China. It lists 12 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 21, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004496806
- Address
- The 3RD Industrial Park Bitou Village, Song Gang Town, BAOAN DISTRICT, SHENZHEN Guangdong, China, 518105
- Owner or operator
- HL CORP. (SHENZHEN) (9062039)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- March 16, 2004
- Registered through
- 2026
- Brand names listed
- HL Adaptor, Hygiene, HL BeD Rail, HL Cane, HL Mechanical walker, HL Transport Wheelchair, HL WHEELCHAIR BRAKE, EXTENSION, HL Wheelchair Anti-tip, HL Wheelchair Armrest and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Hygiene | ILS | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Armrest, Wheelchair | IML | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Brake, Extension, Wheelchair | IMW | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Cane | IPS | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Chair, With Casters | INM | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Cushion, Wheelchair | IMP | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Device, Anti-Tip, Wheelchair | IMR | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Footrest, Wheelchair | IMM | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | 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 |
|---|---|---|---|---|---|---|
| September 21, 2007 | K072311 | TILITE AERO X | IOR | Substantially Equivalent | Tisport, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Wheelchair, Mechanical
- All makers of Adaptor, Hygiene
- All makers of Components, Wheelchair
- All makers of Footrest, Wheelchair
- All makers of Cane
- All makers of Brake, Extension, Wheelchair
Updated September 21, 2007. 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.