Data / Medical devices / China / Seic Shenzhen Shinelong Electronics Industrial Co.
Seic Shenzhen Shinelong Electronics Industrial Co.: FDA-registered device maker in Long Gang District,, SHENZHEN Guangdong, China, 1 510(k) clearance
Seic Shenzhen Shinelong Electronics Industrial Co. is registered with the FDA (registration 3004779467) in Long Gang District,, SHENZHEN Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 6, 2002. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004779467
- Address
- 5/F, Buillding A, Plant No.4, No.1 New Energy Road, Bao Long Intelligent Manufacturing Park Bao Long Community, Bao Long Street, Long Gang District,, SHENZHEN Guangdong, China, 518116
- Owner or operator
- SHENZHEN SHINELONG ELECTRONICS INDUSTRIAL CO.LTD (SEIC) (9066728)
- Roles
- Contract manufacturer, Exporter to the US
- First device listed
- November 23, 2007
- Registered through
- 2026
- Brand names listed
- Microlight (TM) ML830(R)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy | NHN | 2 | Contract manufacturer, Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| February 6, 2002 | K010175 | MICROLIGHT 830 LASER SYSTEM | NHN | Substantially Equivalent | Microlight Corporation of America | accessdata.fda.gov |
Compare with other makers
Updated February 6, 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.