Guangdong Prestige Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Guangdong Prestige Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Electric Scooter (S202572J, S2060, M2089, S2050), Electric Scooter (M2085, S2091), Electric Scooter (Model: M2020)
4
Total
4
Cleared
0
Denied
Guangdong Prestige Technology Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Dongguan, CN.
Latest FDA clearance: Dec 2025. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Guangdong Prestige Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Share Info (Guangzhou) Medical Consultant , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Guangdong Prestige Technology Co., Ltd.
4 devices
Cleared
Dec 23, 2025
Electric Scooter (S202572J, S2060, M2089, S2050)
Physical Medicine
109d
Cleared
Jul 16, 2024
Electric Scooter (M2085, S2091)
Physical Medicine
167d
Cleared
Jul 05, 2023
Electric Scooter (Model: M2020)
Physical Medicine
183d
Cleared
May 05, 2023
Electric Scooter (Model: S3312)
Physical Medicine
60d