Data / Medical devices / China / Shenzhen Launch Electrical Co., Ltd
Shenzhen Launch Electrical Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances
Shenzhen Launch Electrical Co., Ltd is registered with the FDA (registration 3007770159) in Shenzhen Guangdong, China. It lists 8 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 23, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007770159
- Address
- Building No. 2, Precision Intelligent Manufacturing Building, No. 8 Jianyou Road Dafu Community, Guanlan Street, Longhua District, Shenzhen Guangdong, China, 518110
- Owner or operator
- Shenzhen Launch Electrical Co., Ltd (10029699)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- June 17, 2009
- Registered through
- 2026
- Brand names listed
- 2104722-001 Trunk Cable 10-Lead IEC, 2104723-001 Trunk Cable 10-Lead AHA, 2104724-001 Leadwire Set, Base 10, DCAR, Banana, AHA., 2104724-002 Leadwire Set, Base 10, DCAR, Banana, IEC., 2104724-005 Lead wire Set, Base 10, Banana, AHA, 2104724-006 Lead wire Set, Base 10, Banana, IEC, 2104724-007 Lead wire Set, Base 10, Banana, IEC, 2104725-001 Leadwire Set, Add-on, DCAR, Grabber, AHA-HEIM. and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cable, Electrode | IKD | 2 | Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Electrode, Electrocardiograph | DRX | 2 | Manufacturer | accessdata.fda.gov |
| Electrode, Needle | GXZ | 2 | Contract manufacturer | accessdata.fda.gov |
| Electrode, Pacemaker, Temporary | LDF | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Electrical, Evoked Response | GWF | 2 | Contract manufacturer | accessdata.fda.gov |
| Stimulator, Nerve | ETN | 2 | Contract manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Peripheral, Electric | KOI | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| January 23, 2025 | K241199 | Rotatable Connector (5944RL) | LDF | Substantially Equivalent | Shenzhen Launch Electrical Co., Ltd. | accessdata.fda.gov |
| December 10, 2018 | K181967 | Disposable Temperature Probe | FLL | Substantially Equivalent | Shenzhen Launch Electrical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Continuous Measurement Thermometer
- All makers of Electrode, Pacemaker, Temporary
- All makers of Cable, Electrode
- All makers of Electrode, Needle
- All makers of Stimulator, Nerve
- All makers of Stimulator, Nerve, Peripheral, Electric
Updated January 23, 2025. 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.