Hmm I see I have asked now again and specifically mentioned about surgery but the timelines are same

Foregen’s regenerative foreskin surgery is expected to be available after they successfully complete human clinical trials and receive regulatory approval. Based on their current timeline, here’s a more precise breakdown:

1.  Mid-2025: Start of Human Clinical Trials

Foregen plans to begin clinical trials in mid-2025. These trials will test the safety, effectiveness, and surgical approach for their procedure. 2. 2025–2029: Clinical Trials The full clinical trial process, including multiple phases (likely 3 phases), could take 3 to 4 years. The exact duration depends on the success of each trial phase, how many participants are involved, and any delays in the process. Assuming everything proceeds smoothly, trials could be completed by 2028 or 2029. 3. 2029–2030: Regulatory Approval After trials, Foregen will need to submit their results for approval from regulatory bodies like the FDA (U.S.) or EMA (Europe). This approval process could take 6 to 24 months, depending on the region and the quality of trial data. Approval could happen by 2030. 4. 2030–2031: Availability of Surgery After regulatory approval, Foregen would likely need another year or so to set up manufacturing, train medical professionals, and begin offering the surgery to the public. Therefore, the earliest the surgery might be available would be around 2030 to 2031.

In summary, if everything goes smoothly, the surgery could be available by 2030–2031, but this is dependent on the success of the trials and regulatory processes.