Amy Miller

Amy Miller, MD

Dr. Amy Miller, our board-certified physician, is a 1996 graduate of the St. Louis University School of Medicine. She has been practicing aesthetics, laser surgery, and nontraditional dermatology since January 2004 at her office in Des Peres, MO. She is an adjunct professor of family medicine and teaches interested medical students and residents the art and science of aesthetic medicine. She is also a national trainer for advanced injection techniques and teaches physicians from around the country how to use medical lasers in their aesthetic practice.

A former Miss Seattle and Mrs. Missouri International, Dr. Miller helps people from all over the world discover their own beauty. Dr. Miller and her staff offer a wide variety of aesthetic procedures to enhance and highlight your own natural beauty. It is her goal to help you feel comfortable in your own skin, look your very best, and empower you to have the confidence to succeed in a competitive world.

She assists women and men from all over the world in discovering the potential that aesthetic medicine has to offer and knows, from experience, that the resulting improvements on the outside have a positive effect on a person’s inner voice and perception of themselves. She helps remove negative perceptions that people feel about themselves when looking in the mirror and empowers them to be confident in themselves and their abilities.

This has led her to be named Top Aesthetic Medicine Specialist in the United States in the winter of 2013. This award recognizes her expertise in helping their 61,412 members. She also won the Best Facial Injectable Filler at the Annual Aesthetic Awards in May of 2013. Dr. Miller has taught both nationally and internationally. In September of 2017, she was invited to attend the EuroMediCom conference in Monaco where she entered to win Best Non-Surgical Facial Rejuvenation. In 2017, Dr. Miller traveled to London to speak at an international conference and she was invited to Monaco as she was “short listed” as a finalist for an aesthetic award for the Best Non-Surgical Facial Rejuvenation. She has been published in the Nursing Aesthetic journal as well. Dr. Miller is married and the mother of three boys.

Amy Miller, MD
13100 Manchester Rd. Suite 250
Des Peres MO 63131
United States
Phone: (314)-543-4015
Url: http://www.stlouisskin.com/

Important Safety Information

Bellafill®
Bellafill® is indicated for the correction of nasolabial folds and moderate to severe, atrophic, distensible facial acne scars on the cheek in patients over the age of 21 years. Patients who have had a positive reaction to the Bellafill® Skin Test, have a history of severe allergies, have known bovine collagen allergies, are allergic to lidocaine, have bleeding disorders or are prone to thick scar formation and/or excessive scarring should not receive Bellafill®. The safety of Bellafill® for use during pregnancy, breastfeeding, or in patients under 21 has not been established. You may experience temporary swelling, redness, pain, bruising, lumps/bumps, itching, and discoloration at the treatment site. These side effects are usually transient and typically resolve within 1–7 days. You may experience lumps/bumps/papules that may occur more than one month after injection and that may persist. Less common side effects include rash and itching more than 48 hours after treatment, persistent swelling or redness, lumps/bumps, acne, and increased sensitivity at treatment sites. Infrequently, granulomas may occur and may be treated by your licensed physician provider. Be sure to call your licensed provider immediately if you notice any unusual skin reactions around the treatment area. Based on the 5-year Post-Approval Study on nasolabial folds with 1,008 patients, long-term safety of Bellafill® for up to 5 years has been established.

PUREGRAFT
This product is certified as a medical device in the European Union under the Medical Device Directive 93/42/EEC by SGS CE0120, exclusively for the indication of autologous fat transfer. Other non-medical uses ascribed to this device such as aesthetic body contouring are not within the scope of CE certification, and users should be aware product performance and/or safety has not been evaluated by SGS for those purposes.

Suneva Medical HD PRP
REGULATORY STATUS: FDA-cleared 510(k) Class II medical device. Healeon HD PRP is designed to be used for the safe and rapid preparation of autologous platelet-rich-plasma (PRP) from a small sample of peripheral blood at the patient point of care. The PRP is mixed with autograft and/orallograft bone prior to application to a bony defect for improving handling characteristics. 510(k) number: BK170136

Silhouette Instalift
Silhouette lnstaLift® is indicated for use in mid-face suspension surgery to temporarily fixate the cheek sub-dermis in an elevated position.

IMPORTANT SAFETY CONSIDERATIONS
The Silhouette InstaLift device should not be used in patients with any known allergy or foreign body sensitivities to plastic/ biomaterial or in situations where internal fixation is otherwise contraindicated, (e.g. infection.) The device should also not be used in patients appearing to have very thin soft tissue of the face in which the implant may be visible or palpable.

Like all procedures of this type there is a possibility of adverse events, although not everybody experiences them. These adverse events include but are not limited to infection, minimal acute inflammatory tissue reaction, pain (which may be temporary or persistent in nature), swelling and edema, transient hematoma or bruising and transient rippling or dimple formation. For further safety or product information, please consult your physician.

For more safety information, please consult with your physician and the patient labeling that can be found by visiting our website www.bellafill.com.
Toll-free call (U.S. & Canada): 844-Bellafill (844-235-5234).
Local calls: 858-550-9999. International calls: ++ 858-550-9999.