ARMS Medical
The Better Question

Pelvic Floor Surgery Technology includes the devices, materials and procedural solutions used to support the repair and reconstruction of pelvic anatomy. The category covers technologies that help surgeons address tissue support and anatomical restoration while working within a complex surgical environment. Effective solutions must account for tissue characteristics, surgical technique and the specific anatomy involved. Pelvic Floor Surgery Technology therefore extends beyond structural support alone and includes how a material is processed, prepared and configured for use during a procedure.

Pelvic Floor Surgery Technology should be evaluated by considering material characteristics, anatomical fit and the preparation required before use. In reconstructive procedures, a product’s geometry can affect how easily it fits the intended application, while tissue processing can influence its biological properties. Technologies that arrive in a prepared configuration may also reduce certain operating room tasks without changing the surgeon’s responsibility for procedural decisions. Evaluation should focus on whether the design, material and workflow align with the specific reconstructive approach rather than treating all pelvic floor repair technologies as interchangeable.

Pelvic Floor Surgery Technology can influence workflow by addressing preparation before a product enters the sterile field. Traditional graft preparation may require the surgical team to hydrate, measure and cut tissue into a desired configuration. Precut, hydrated products can shift some of those steps into product design and manufacturing, allowing the surgeon to focus on selecting the appropriate configuration and determining placement. The practical value depends on the procedure and surgical technique, but thoughtful preparation can reduce unnecessary handling while maintaining flexibility during reconstruction.

ARMS Medical has developed its approach through extensive time spent in operating rooms with urogynecologists, urologists and colorectal surgeons, using those interactions to understand the challenges involved in pelvic floor reconstruction. VNEW technology has since been used by more than 200 surgeons in the care of more than 10,000 women. ARMS Medical combines that clinical experience with a product strategy centered on anatomical shapes, mesh-free dermal allograft material and tissue-processing technology. This continued interaction with surgeons helps inform how Pelvic Floor Surgery Technology can address practical reconstructive needs.

Tissue processing can play an important role in Pelvic Floor Surgery Technology because the biological properties of a graft may depend on how the tissue is prepared. VNEW uses patented processing technology originally developed for tissue intended for heart valve replacement. The process removes more than 99 percent of donor DNA while preserving key components of the native extracellular matrix, including collagen and vascular channels. In pelvic floor reconstruction, this type of technology must work alongside anatomical design and surgical judgment rather than being considered separately from the procedure.

ARMS Medical applies Pelvic Floor Surgery Technology by designing VNEW around female anatomy rather than adapting an existing graft for pelvic floor reconstruction. The company offers a patented, mesh-free dermal allograft in four precut anatomical shapes, allowing surgeons to select a configuration suited to the procedure. VNEW also arrives hydrated and ready for use, reducing preparation steps that can otherwise involve soaking, measuring and cutting tissue in the operating room. This approach combines anatomical design with a workflow intended to simplify preparation while preserving surgeon control over technique and placement.