FDA Clears Twiist Automated Insulin Delivery System
DEKA Research and Development Corp has received 510(k) clearance FDA for the twiist Automated Insulin Delivery system powered by Tidepool.
Read MoreMar 18, 2024 | Clearances | 0 |
DEKA Research and Development Corp has received 510(k) clearance FDA for the twiist Automated Insulin Delivery system powered by Tidepool.
Read MoreFeb 28, 2024 | Company News | 0 |
Know Labs, detailed the features of the KnowU, a wearable non-invasive continuous glucose monitor that can connect to a mobile app.
Read MoreJul 17, 2023 | FDA Updates, Ultrasound | 0 |
The U.S. FDA is warning against unsafe ultrasound devices from RoyalVibe Health, CellQuicken, and Well-Being Reality, citing potential dangers, lack of FDA review, and risks of adverse effects.
Read MoreJul 14, 2023 | Clearances | 0 |
FDA has cleared the Tandem Mobi insulin pump for people with diabetes age 6 and up. The small device is fully controllable from a mobile app.
Read MoreJun 26, 2023 | Remote Monitoring | 0 |
The wearable device is worn around the waist and painlessly and automatically samples from beneath the skin every 20 minutes, without the need to collect blood.
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