
Ova1Plus® – Aspira Women's Health
Ova1Plus is a proprietary reflex process combining two FDA-cleared tests, Ova1 ®, leveraging high sensitivity, and Overa ®, leveraging high specificity, for patients with adnexal masses.
iovera | Non-Opioid Pain Relief Treatment
FDA-cleared iovera provides immediate pain relief using cryoneurolysis. Drug-free treatment for knee, hip, shoulder, spine & more. Lasts up to 90 days.
Overa - Early Detection Research Network
From Vermillion website: Overa, a second-generation Multivariate Index Assay (MIA2G) is an FDA-cleared blood test for women with a pelvic mass who are planned for surgery.
Overa 2026 Company Profile: Valuation, Funding & Investors
Information on valuation, funding, cap tables, investors, and executives for Overa. Use the PitchBook Platform to explore the full profile.
Overa 00860942000106 Medical Device Identification
The Overa® test is intended to aid in assessing whether a woman who presents with an ovarian adnexal mass is at high or low likelihood of finding malignancy as part of the preoperative …
Ovarian Cancer Testing - GenPath
Ova1Plus is a reflex process which performs Ova1 ® and Overa ®, both FDA-cleared tests for women with adnexal masses planned for surgery. What are the benefits of Ova1Plus®?
FAQs – Aspira Women's Health
No, you do not need to order Overa separately. When you order Ova1Plus, Overa will automatically be performed if the Ova1 result falls into the intermediate-risk category.
OVERA - Architecture AI Assistant - Facebook
OVERA - Architecture AI Assistant. 485 likes · 29 talking about this. OVERA is an AI-powered assistant built for architects and designers. It transforms...
Aspira Women’s Health, BioReference to distribute blood tests to …
The firms will co-market and distribute Aspira’s Ova1Plus, which combines its U.S. Food and Drug Administration-cleared blood tests, Ova1 and Overa, to detect the risk of ovarian malignancy …
Aspira Women’s Health Announces Publication of its
Sep 12, 2022 · The study concluded that incorporating MIA2G (OVERA) rather than CA-125 into clinical assessment would increase the detection of early-stage ovarian cancers, regardless of …