Scott Callahan

Scott Callahan, PA-C

Scott is a Physician Assistant who founded Dolce Vida Medical Spa in 2010 with the primary goal of helping people maintain a vibrant, youthful appearance. His mission is to assist people to feel great about their personal presentation and to boost their self-esteem.

He specializes in enhancing, corrective procedures and facial filler administration with a keen, discerning eye for detail. Scott is well known for his knowledge, skill and expertise with just the right filler placement in order to deliver a refreshed, natural-looking result. This has contributed to his notoriety and he is currently the top (#1) injector in the entire state of Connecticut. Scott is the expert trainer/educator for multiple companies including Suneva, Galderma, Harvest Terumo and Merz. He is a trainer/educator for Bellafill for the East Coast and was the very first injector of Bellafill in the state of Connecticut. He has been featured on multiple local and network television shows including a featured spot on The Style Network.

Scott shares his knowledge and expertise as a lecturer/speaker at multiple aesthetic medical conferences throughout the country. He is highly skilled with cannula techniques, fat transfer procedures, PRP injectables, resurfacing laser techniques, lip augmentation, tear trough eye correction and Botox brow lifts. Scott has worked in the medical field for more than 16 years and has past experience in Plastic Surgery, General Surgery and Pediatric/Adult Cardiac Surgery. His professional manner and his highly skilled knowledge base has helped to contribute to his success with achieving great results and complete client satisfaction. He is known for spending extra time with each client to achieve the best results possible, as he views each individual as special with unique needs. Scott is a highly regarded mentor, exceptional practitioner and leading authority in the field of Aesthetic Medicine.

Scott Callahan, PA-C
1799 Post Rd. E
Westport CT 06880
United States

Important Safety Information

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.

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.

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
Toll-free call (U.S. & Canada): 844-Bellafill (844-235-5234).
Local calls: 858-550-9999. International calls: ++ 858-550-9999.