The IUB® SEAD® (Spherical Endometrial Ablation Device) – currently in Phase II Clinical Studies – offers a disposable, point of care therapy for abnormal uterine bleeding (AUB) and/or heavy menstrual bleeding – a far more comfortable and cost effective alternative for hundreds of thousands of women per year who opt to increase their quality of life.
14 – 25% of women
of reproductive age
are affected by AUB
42% of women suffer
from depression
due to heavy periods
The IUB® SEAD® is an innovative intrauterine drug delivery technology for women with abnormal uterine bleeding and/or heavy menstrual bleeding. The current standard of care (global endometrial ablation) is considered invasive, burdensome, debilitating, and costly and may result in uterine wall adhesions and even a hysterectomy.
Current global ablation technologies currently in use require expensive capital equipment, extensive physician training, general anesthesia & hospitalization and cause high indirect costs and usually pain to women.
The IUB® SEAD® is a market game-changer through simplicity, cost-effectiveness, and new and innovative yet gentle “substance-derived ablation” technology. The IUB® SEAD® is nearly pain-free2 and efficacious to reduce bleeding and increase the quality of life.
The data presented at the 2021 FIGO World Congress on OCON’s IUB® SEAD® (Spherical Endometrial Ablation Device) shows over 80% reduction in bleeding with 95% of women reporting quality of life satisfaction.” Prof. Sergio Haimovich, CMO.
The IUB® SEAD® is a market game-changer through simplicity, cost-effectiveness, and new and innovative yet gentle “substance-derived ablation” technology.
Phase I Clinical Studies have successfully demonstrated safety3. Phase II Clinical Studies are currently ongoing.
The IUB® SEAD® has the potential of becoming a strong and attractive choice of therapy in the worldwide GEA market through its simplicity, cost effectiveness and new and innovative yet gentle “substance-based Ablation” technology.
2 ongoing Phase II Clinical Studies, OCON Medical Ltd.
3 Phase I Clinical Study, OCON Medical Ltd.