Nu-Beca & Maxcellent Co. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Nu-Beca & Maxcellent Co. - FDA 510(k) Cleared Devices
Recent clearances: Nu-beca Transcutaneous Electrical Nerve Stimulation
1
Total
1
Cleared
0
Denied
Nu-Beca & Maxcellent Co. has 1 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Nu-Beca & Maxcellent Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Taidoc Technology Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Nu-Beca & Maxcellent Co.
1 devices