Not currently registered with FDA under this name

Neo Group Limited

Hung Hom, Kowloon, Hong Kong SAR China. Named as applicant on 1 dental 510(k) clearance between 2013 and 2013. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12013–2013
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Neo Group Limited as the applicant.

Decided	510(k)	Device	Device type
21 Oct 2013	K130198	NEO DENTA ZIRCONIA	EIH Porcelain Powder

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.