Quanta System Spa is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quanta System Spa - FDA 510(k) Cleared Devices
Recent clearances: Discovery Pico, Single Use CO2 Laser Fiber (HAF005001), Youlaser PRIME
57
Total
57
Cleared
0
Denied
Quanta System Spa has 57 FDA 510(k) cleared general & plastic surgery devices. Based in Chelmsford, US.
Latest FDA clearance: Jun 2025. Active since 2006.
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 Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Quanta System Spa
57 devices
Cleared
Jun 06, 2025
Discovery Pico
General & Plastic Surgery
422d
Cleared
Feb 19, 2025
Single Use CO2 Laser Fiber (HAF005001)
General & Plastic Surgery
91d
Cleared
Oct 10, 2024
Youlaser PRIME
General & Plastic Surgery
171d
Cleared
Sep 03, 2024
Litho 60
General & Plastic Surgery
34d
Cleared
Oct 20, 2023
Echo
General & Plastic Surgery
85d
Cleared
Jan 20, 2023
Duetto Suprema
General & Plastic Surgery
72d
Cleared
Mar 16, 2022
Fiber Dust PRO
General & Plastic Surgery
30d
Cleared
Feb 02, 2022
Rosso
General & Plastic Surgery
285d
Cleared
Mar 11, 2021
Fiber Dust
General & Plastic Surgery
51d
Cleared
Nov 18, 2020
Chrome
General & Plastic Surgery
79d
Cleared
Oct 15, 2020
Opera Evo
General & Plastic Surgery
84d
Cleared
Jun 30, 2020
Litho 150, Cyber Ho 150
General & Plastic Surgery
29d
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