Bioinfinity (M) Sdn. Bhd. is one of 15156 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioinfinity (M) Sdn. Bhd. - FDA 510(k) Cleared Devices
Recent clearances: Vibrance Pelvic Trainer, VIBRANCE KEGEL DEVICE (VKD)
2
Total
2
Cleared
0
Denied
Bioinfinity (M) Sdn. Bhd. has 2 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 2 cleared submissions from 2014 to 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Bioinfinity (M) Sdn. Bhd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Group as regulatory consultant.
FDA 510(k) Regulatory Record - Bioinfinity (M) Sdn. Bhd.
2 devices