Dr. James DeYarman


Since 1974, Dr. James DeYarman has studied and developed new techniques in hair restoration. Dr. DeYarman, brings over 40 years of experience in the field of Hair Transplant surgery. With creative approach and advocacy, Dr. DeYarman evolves into a premier hair transplant surgeon and specialist in the hair restoration field. In addition, has written and lectured extensively on the topic of hair loss. Dr. DeYarman incorporates an artistic approach to hair transplants, giving patients a natural-looking hairline, which has heralded him a leader in his field. With innovative methods Dr. DeYarman has been able to provide the most natural-looking hairline for his patients.

Dr. James DeYarman graduated from Northeast Missouri State with a Bachelor of Science degree in 1969. In 1973, he graduated from Kirksville College of Osteopathic Medicine. He completed his rotating internship in general practice at Doctors Hospital in Tucker, Georgia. Dr. DeYarman began a general practice in 1974 in San Diego, California. During this time, he became interested in hair restoration. In 1978, Dr. DeYarman did a preceptorship with Dr. C.P. Chambers of Tampa, Florida in the art of hair transplantation.

Dr. James DeYarman, owner of DeYarman Medical Group, has been performing Hair Restoration for Men and Women for over 40 years. Offering Robotic Hair Transplant, conventional methods including manual FUE, ‘strip’ surgery and Stem Cell Hair Therapy.
Dr. DeYarman focused on hair transplant from the beginning of his medical career and reveals how Stem Cell Hair Therapy is the game-changer for hair restoration.

Dr. DeYarman is licensed to practice medicine in the following states: California, Hawaii, Nevada, Utah, Tennessee, and Florida. He is currently a member of the National A.O.A., California Osteopathic Association, San Diego Osteopathic Association, American Society of Hair Restoration Surgery, International society of Hair Restoration Surgery, American Academy of Cosmetic Surgery, and a past board member of the California State Association (O.P.S.C.).


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Individuals interested in any cellular or cell-free regenerative medicine therapy are urged to review all pertinent information and do their own research and due diligence before choosing to participate in any therapies. Please consult with your physician for further information and be sure to discuss any potential risks.

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This site was intended for education purposes only and strictly for use by medical professionals. The FDA recently re-confirmed, there is only one registered stem cell product, and while there is enormous promise in stem cell therapies, and thousands of ongoing experimental applications trying to establish efficacy, these are not at the point where they would meet the scientific standard.

The FDA has stated:
Stem cells, like other medical products that are intended to treat, cure or prevent disease, generally require FDA approval before they can be marketed. FDA has not approved any stem cell-based products for use, other than cord blood-derived hematopoietic progenitor cells (blood forming stem cells) for certain indications.

This site is not intended for consumers.
If you are considering stem cell treatment in the U.S., ask your physician if the necessary FDA approval has been obtained or if you will be part of an FDA-regulated clinical study. This also applies if the stem cells are your own. Even if the cells are yours, there are safety risks, including risks introduced when the cells are manipulated after removal.

“There is a potential safety risk when you put cells in an area where they are not performing the same biological function as they were when in their original location in the body.” Cells in a different environment may multiply, form tumors, or may leave the site you put them in and migrate somewhere else. If you are considering having stem cell treatment in another country, learn all you can about regulations covering the products in that country. Exercise caution before undergoing treatment with a stem cell-based product in a country that—unlike the U.S.—may not require clinical studies designed to demonstrate that the product is safe and effective. FDA does not regulate stem cell treatments used solely in countries other than the United States and typically has little information about foreign establishments or their stem cell products.

Stem cell therapies have enormous promise, but the science in each use is still in the developmental stage. Professional judgment and expertise is needed in using stem cells for any therapeutic use, and we urge anyone embarking on the use of stem cell therapies to consult the national health data bases to evaluate current information from clinical trials and the FDA websites on human tissue should also be consulted to get its current evaluation of any therapy.