Data / Medical devices / China / JSL Car Accessories Co., Ltd.
JSL Car Accessories Co., Ltd.: FDA-registered device maker in Shanghai, China, 1 510(k) clearance
JSL Car Accessories Co., Ltd. is registered with the FDA (registration 3004993527) in Shanghai, China. It lists 17 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 16, 2002. Registered through 2026. 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
- 3004993527
- Address
- 5/F, Huanan Mansion No.1988 Dongfang RD, Shanghai, China, --
- Owner or operator
- JSL CAR ACCESSORIES CO., LTD. (9098271)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- February 27, 2007
- Registered through
- 2026
- Brand names listed
- Dukal, Lifeline First Aid, Lifeline, AAA, MULTIPLE, MUTIPLE, Ningo Asian-Pacific Oprical Instrument, SURGICAL BLADE, Zhenjiang YinYu Paper Industry and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Absorbent Tipped, Non-Sterile | KXF | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Bandage, Elastic | FQM | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Blade, Scalpel | GES | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Depressor, Tongue, Non-Surgical | FMA | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| First Aid Kit With Drug | LRR | N | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| First Aid Kit Without Drug | OHO | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Forceps | HTD | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pack, Hot Or Cold, Disposable | IMD | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Pad, Eye | HMP | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Sling, Arm, Overhead Supported | ILE | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Vinyl Patient Examination Glove | LYZ | 1 | Exporter to the US, Repackager or relabeler | 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 16, 2002 | K022600 | POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES | LYZ | Substantially Equivalent | Shijiazhuang Wally Plastics Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Fiber, Medical, Absorbent
- All makers of Applicator, Absorbent Tipped, Non-Sterile
- All makers of First Aid Kit With Drug
- All makers of Blade, Scalpel
- All makers of Depressor, Tongue, Non-Surgical
- All makers of Disinfectant, Medical Devices
Updated September 16, 2002. 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.