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Vacuum erection devices (VEDs) are FDA-cleared treatment options for erectile dysfunction and post‑prostatectomy rehabilitation; FDA guidance requires safety features such as quick‑release/pop‑off val...
Vacuum erection devices (VEDs) have been FDA-cleared for treatment of erectile dysfunction since the early 1980s and are available from multiple manufacturers, but no single, exhaustive list of every ...
Vacuum erection devices (VEDs, aka penis pumps) are available both by prescription and over the counter: many clinical and hospital sources say VEDs can be prescribed by urologists and covered by insu...
No single, consolidated public list in the supplied sources names which vacuum erection device (VED) models are FDA‑cleared in 2025; the FDA maintains searchable 510(k) clearance records that include ...
Clinical and regulatory backing for vacuum erection devices (penis pumps) exists, but it applies to the device class rather than specific consumer-brand claims: the FDA treats vacuum pumps as Class II...
A narrow set of medical vendors and clinical resources repeatedly identify specific vacuum erection device (VED) models as “FDA‑cleared” — notably Augusta Medical’s SomaTherapy Manual and SomaTherapy ...
Vacuum erection devices (VEDs) are an established, FDA‑regulated class of medical devices used to treat erectile dysfunction and for penile rehabilitation; the FDA has classified them as Class II devi...
Anticoagulant medications raise the likelihood and potential severity of bleeding and bruising when using a vacuum erection device (VED), and this risk shapes conservative clinical counsel: discuss an...
A focused review of the provided reporting finds no peer‑reviewed clinical trials that explicitly evaluate the devices Pos‑T‑Vac, Vacurect, VaxAid, or menMD by model name; the materials are primarily ...
There are no explicit, documentable FDA recalls for vacuum erection devices (VEDs) in the material provided here, but the FDA has issued device-specific guidance and safety labeling expectations that ...
A small set of commercially marketed vacuum erection devices (VEDs) hold FDA 510(k)-era clearances or are registered in federal device databases, but public documentation varies: Imagyn Medical’s Irnp...
A number of vacuum erection devices (VEDs) are sold in the United States with manufacturers’ or sellers’ claims of FDA clearance; public records and vendor pages in the reporting identify specific mod...
Vacuum erection devices (VEDs) are widely described in clinical and consumer sources as an effective, non‑invasive option for erectile dysfunction when used per manufacturer and clinical guidance; reg...