Evaluation of the Nella Women's Care Line

General inclusion criteria (applies to all study groups): * Subject is female * Subject is 18 - 65 years of age, inclusive, at the time of consent * Subject is undergoing a gynecological examination (as defined above) as part of their regular clinical care * Subject has undergone one or more prior gynecological exams * Subject is willing and able to provide written informed consent * Subject is able and willing to perform the functions required by the study protocol General exclusion criteria (applies to all study groups): * Subject has undergone hysterectomy * Subject has a known history of allergies to latex or plastics * Subject is pregnant * Subject is post-partum (≤ 12 weeks) * Subject has had an induced or spontaneous abortion in the prior 12 weeks * Subject has an active gynecologic complaint that, in the opinion of the clinician, would confound study results * Subject has dyspareunia * Subject has a known history of vulvodynia such as vulvular vestibular syndrome * Subject has a known history of vaginismus * Subject has a planned surgical procedure along with the gynecological exam * Subject is under incarceration * Subject is unable to provide written informed consent Device specific inclusion criteria: In addition to the general inclusion, the subject must meet all device specific criteria associated with their assignment group. Below are device-specific criteria. There is no device-specific exclusion criterion. Nella VuSleeve (Group 1) inclusion: • Subject has a BMI ≥ 30 and/or 3 or more vaginal births NellaSpec (Group 2), Nella NuSpec (Group 3), and Nella Insert (Group 4) inclusion: • Subject has a BMI \< 35