KAI Xing Optical Limited

Registered establishment in Guangdong, China. 4 device types.

Registry build 21.09.26

KAI Xing Optical Limited is a manufacturer holding a current FDA establishment registration. The registration covers Frame, Spectacle, Spectacle, Magnifying and 2 other device types. Its earliest product listing with the FDA dates from 2003.

Registration

FDA registration record for KAI Xing Optical Limited
Registered name KAI XING OPTICAL LIMITED
Status Registered
Registration expires 2026
Registration number 3001135633
FEI number 3001135633
Establishment type Manufacturer

Location

Address of KAI Xing Optical Limited
City Guangdong
Province Guangdong
Address JIN PAI SHAN, TAI YANG AO
Postal code 516369
Country China

What It Makes

Device types KAI Xing Optical Limited is registered to make
Device type Class Listed under the names Listed since Chinese makers
Frame, Spectacle Class 1 Spectacle#ophthalmology 2003 430
Lens, Spectacle, Non-Custom (Prescription) Class 1 Lens 2024 263
Spectacle, Magnifying Class 1 Magnifying#ophthalmology 2003 360
Sunglasses (Non-Prescription Including Photosensitive) Class 1 2003 522

Nearby Manufacturers

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

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Where China Actually Supplies

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2,581device types they are registered for
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