Abbott just put physiologic pacing and defibrillation on one lead. Can UltiSynq change how ICDs are implanted?
Abbott’s UltiSynq wins FDA approval and CE Mark after 98.5% implant success and 100% successful tested defibrillation in ASCEND CSP.
Abbott’s UltiSynq wins FDA approval and CE Mark after 98.5% implant success and 100% successful tested defibrillation in ASCEND CSP.
Abbott has reported 97% procedural success and 0.3% target lesion failure at 30 days in its 335-patient TECTONIC study of SonicForce. The findings support the investigational system's regulatory development, although the single-arm trial does not establish superiority over existing coronary lithotripsy devices.
Teleflex completes BIOMAG-LL enrollment in 102 patients, testing longer Freesolve magnesium scaffolds ahead of European regulatory expansion.
Ascensia backs Sava's $36M glucose microsensor push, but clinical validation and CE marking remain critical before its planned European launch.
Abbott Laboratories (NYSE: ABT) has received United States Food and Drug Administration approval for new patient-facing capabilities within its CardioMEMS HF System, allowing care teams to give patients access to pulmonary artery pressure trends through the CardioGuide HF App. The update also introduces a Dynamic Treatment Plan feature through which clinicians can communicate personalised medication
Abbott Laboratories has received FDA approval for TactiFlex Duo, a focal ablation catheter capable of delivering both pulsed-field and radiofrequency energy. The system enters a rapidly expanding pulsed-field ablation market with a different proposition: instead of replacing thermal ablation entirely, it lets electrophysiologists choose between energy types during the same procedure.
Abbott’s TactiFlex Duo combines pulsed field ablation and radiofrequency energy in one contact-force catheter, giving electrophysiologists a way to move between tissue-selective PFA and conventional thermal ablation without changing platforms during an AFib procedure.
Abbott Laboratories has secured FDA De Novo authorization for Libre Duo 10 Day, the first wearable in the United States to continuously monitor ketones and the first device globally to continuously measure glucose and ketones together.
Avricore Health’s HealthTab will distribute Abbott’s Afinion 2 through NHS-linked pharmacies, combining rapid HbA1c and lipid testing with a connected platform for community-based screening.
FDA approves Freenome’s SimpleScreen CRC blood test as Abbott plans a fall launch. See its benefits, limits and colonoscopy requirement.