Shanghai Apolo Medical Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shanghai Apolo Medical Technology Co., Ltd. - FDA 510(k) Cleared Devi...
Recent clearances: Q-Switched Nd: YAG Laser Systems, Picosecond Nd:YAG Laser Systems (Model: HS-298), Fiber Laser Treatment Systems (HS-232,HS-233)
14
Total
14
Cleared
0
Denied
Shanghai Apolo Medical Technology Co., Ltd. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Shanghai, CN.
Latest FDA clearance: May 2026. Active since 2019.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Landlink Medical Information Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Shanghai Apolo Medical Technology Co., Ltd.
14 devices
Cleared
May 04, 2026
Q-Switched Nd: YAG Laser Systems
General & Plastic Surgery
96d
Cleared
Apr 09, 2026
Picosecond Nd:YAG Laser Systems (Model: HS-298)
General & Plastic Surgery
94d
Cleared
Jul 02, 2025
Fiber Laser Treatment Systems (HS-232,HS-233)
General & Plastic Surgery
90d
Cleared
Apr 10, 2024
Electromagnetic Stimulation Systems
Physical Medicine
244d
Cleared
Oct 13, 2022
Fiber Laser Treatment System
General & Plastic Surgery
114d
Cleared
Jan 28, 2022
Platform treatment system
General & Plastic Surgery
436d
Cleared
Sep 10, 2020
Diode Laser Body Sculpture System
General & Plastic Surgery
78d
Cleared
Jul 15, 2020
CO2 Laser Therapy System
General & Plastic Surgery
79d
Cleared
May 28, 2020
PicoSecond Nd: YAG Laser System
General & Plastic Surgery
128d
Cleared
May 15, 2020
IPL Treatment Systems
General & Plastic Surgery
53d
Cleared
Apr 17, 2020
Diode Laser Therapy Device
General & Plastic Surgery
87d
Cleared
Aug 16, 2019
980nm Diode Laser Therapy Device
General & Plastic Surgery
88d