Regenerative Curative Preventative InvestorPresentation Safe Harbor 1 Statements in this presentation that are not descriptions of historical facts are forward-looking statements relating to future events, and as such all forward-looking statements are made pursuant to the Securities Litigation Reform Act of 1995. Statements may contain certain forward-looking statements pertaining to future anticipated or projected plans, performance and developments, as well as other statements relating to future operations and results. Any statements in this presentation that are not statements of historical fact may be considered to be forward-looking statements. Words such as "may," "will," "expect," "believe," "anticipate," "estimate," "intends," "goal," "objective," "seek," "attempt," or variations of these or similar words, identify forward-looking statements. These forward-looking statements by their nature are estimates of future results only and involve substantial risks and uncertainties, including but not limited to risks associated with the uncertainty of future financial results, additional financing requirements, development of new products, successful completion of the Companys proposed restructuring, the impact of competitive products or pricing, technological changes, the effect of economic conditions and other uncertainties detailed from time to time in our reports filed with the Securities and Exchange Commission. There can be no assurance that our actual results will not differ materially from expectations and other factors more fully described in our public filings with the U.S. Securities and Exchange Commission, which can be reviewed at www.sec.gov. INTELLICELL BIOSCIENCES Research began in 2009 and Company founded in 2010 Cellular laboratory in New York and planned location in Florida New facilities and planned in major US markets 2 Cellular Processing Laboratory IntelliCell has first commercial cellular processing laboratory integrated into an ASC suite in NYC Capability to treat multiple disease and injury states under the practice of medicine Facility meets regulatory requirements for cGTP processing Can be deployed in major markets in US and Internationally Hospital/Ambulatory Surgery Center Labs Business Model Business Model The company will install/build a FDA cGTP lab in a 25 x 25 foot room The company will employee a QC technician that it trains and monitors The QA of the lab would be accomplished via NY QA director All SOPs would be handled by Company The Company would sell cells for $2,500 and the physician/hospital would charge patient fee set by them if the hospital pays for the lab BUT if Intellicell pays for lab do a 50/50 revenue share All samples would be total QA Cells available to all and any specialties Company would arrange CME courses 5 Why doctors would use cells Continuing Medical Education The company will conduct continuing medical education course to multiple specialties in order to teach physicians about cellular therapy The CME course will also expose the physicians to the availability of Intellicells cellular product to treat their patients under the practice of medicine 7 Clinical Experience Summary of Results for SVF Treatments OVER 400 PATIENTS TREATED WITH SVF NO ADVERSE REACTIONS TO ANY SVF TREATMENT 4 LOCAL INFECTIONS AT PUNCTURE SITE OF HARVESTING (DUE TO POOR WOUND CARE BY PATIENT) 8 PHYSICIAN GROUP MEDICAL PRACTICE Cosmetic Dermatologist Cosmetic / Plastic Surgeon Ear Nose & Throat Specialist Internal Medicine Specialist 3 Orthopedic Specialists Neuropsychiatrist Anecdotal Clinical Results ALS- QEEG Scans 10 MRI Indicating Positive Changes in OA Hip 11 Skiing fracture 12 MultipleFractures WastoldneverraceagainBUT racing in6months 13 New York Daily News The J ournal of Implant & Advanced Clinical Dentistry 14 Volume Filling & wrinkles 15 FreshFat+SVFs Treatment for Bells Palsy 16 Weeks After Treatment BellsPalsy NerveDroop Nomoredroop 62yroldType1Diabeticdiagnosedwith permanentBellsPalsy Currently Pre- treatmentSeSe One Hour Later MARKET OPPORTUNITY Market Indications $15 billion current market for Regenerative Medicine 1.2 million patients to date treated with RM products and therapies 400 + private and 50 public companies with $4.7 billion in total market cap 175,000 peer-reviewed publications and 10,000 issued or pending patents 400 products in the market today with 600 more in development Proliferation of patient advocacy groups demanding shift to RM $1.5 billion in worldwide research funding projected to $14 billion in 10 years Potential market is LARGELY UNTAPPED Projected to reach $300 billion by 2020 source: US Department of Health and Human Services 19 AND THATS JUST THE BEGINNING Partial List of Potential Treatable Conditions Osteoarthritis Internal Medicine Gum Regeneration Periodontal Diabetic Ulcers Wound healing Multiple Sclerosis Parkinsons Internal Medicine Cartilage Regeneration Severe Burns 20 Orthopedic and Sports Medicine Tendon Repair Facial Lines and Wrinkles Aesthetic Medicine Heart Damage Chronic Migraine Headache Nerve Damage Bone Regeneration General Surgery Hair Regeneration Blindness and Deafness Regenerative Medicine can offer new options and improved outcomes THE INTELLICELL SCIENCE Stromal Vascular Fraction (SVF) Intellicells therapies use Adult Stromal Vascular Cells Derived from Blood Vessels in adipose tissue Capillaries are primary source Same-day clinical procedure High cell counts 22 Blood vessels Adipose (fat) cells Capillaries SVF cellular composition: Adult adipose stem cells Pre-adipocyte cells Endothelial cells Smooth muscle cells Pericytes Fibroblasts Growth factors Blood Cells from capillaries: B &T cells M2 Macrophages (anti-inflammatory) Monocytes Mast cells Natural killer (NK) cells Hematopoietic stem cells Endothelial progenitor cells The Intellicell Process (patent pending) 23 Enzymatic Extraction Ultrasonic Cavitation Typical Method Intellicell Method Typical Manufacturing Process: SVF is manufactured from adipose tissue using collagenase enzymes, particularly Liberase manufactured by Roche Intellicell Innovation: We discovered and pioneered the use of ultrasonic cavitation to manufacture SVF from adipose tissue The IntelliCell Ultrasound Cavitation R & D Over 3 years in development Over 700 tissue samples studied Several mechanical systems tested, ultrasound emerged as best Significant trial and error required to perfect the process Resulted in a process that yields large cell numbers per cc of tissue harvested Resulted in a process that demonstrates high cell viability 24 Ultrasonic Cavitation Enzymatic Extraction Typical Method vs. Intellicell Method 25 Cells per ML: 3-8 Million Dead Cells: 15-30% Debris: 5-15% Total Volume of cells: 20 cc Total Dose: 50-70 Million Cells Cells per ML: 20-30 Million Dead Cells: 5-8% Debris: 2-6% Total Volume of Cells: 40-50 cc Total Dose: 500 Million - 1 Billion COSTOFDISPOSABLES:$150 MANUFACTURINGTIME:45to 60MINUTES COSTOFDISPOSABLES:asmuchas$1500 MANUFACTURINGTIME:60to120MINUTES Extracting SVF from 60 CC of adipose tissue MANUFACTURING PROCESS IntelliCellCell Process 27 Inject into site of ailment Administer intravenously 28 Lab Procedures All SVF manufactured under FDA "current Good Tissue Practices" (cGTP) IntelliCell has a Director of QA to ensure all procedures fully compliant Each specimen produced will have to be released by a QA manager For remote sites we will employ a Modular Clean Room set up or build out a cGTP lab Aseptic Containment Isolator meets all FDA tissue handling requirements 29 Evaluation Using a Flow Cytometer laser that measures cell count and viability Release Criteria for use of SVF FLOW CYTOMETRY: 80%+ Viability ENDOTOXIN TESTING: within standards GRAM STAIN: negative Additional testing: 14-day sterility assay intra-process plating Patent Granted 30 U.S. Patent 8,440,440 & International Patent Application PCT/US2011/64464 "ULTRASONIC CAVITATION DERIVED STROMAL OR MESENCHYMAL VASCULAR EXTRACTS AND CELLS DERIVED THEREFROM OBTAINED FROM ADIPOSE TISSUE AND USE THEREOF" U.S. Provisional Application No. 61/674,116 "ISOLATION OF STROMAL VASCULAR FRACTION FROMADIPOSE TISSUE OBTAINED FROM A NON-LIVING SOURCE USING ULTRASONIC CAVITATION" Intellicell will be filing additional patents Companys Cellular Product FDA FDA Major Conclusion Points Our Lab process falls under FDA CFR 1271.10 (a) and therefore we believe PHS 361 exempt Also the cells are utilized under CFR 1271.15 (b) and any clinical claims are made by the physician under the practice of medicine We operate a fully validated FDA cGTP laboratory with strict SOPs All our cellular samples are subject to strict QA release criteria and our product is sterile and traceable 32 MANAGEMENT & ADVISORS Management 34 Dr. Steven Victor, Chairman and CEO Dr. Steven Victor, founder and CEO of IntelliCell, has been at the forefront of clinical product and process development for over 20 years. The patent pending process that Dr. Victor has developed for IntelliCell has been in research for over 4 years. Dr. Victor is a practicing dermatologist in New York City. Dr. Victor's work in regenerative medicine began over a decade ago upon the start of clinical use of autologous fibroblast cells for the purpose of dermal regeneration. Dr. Victor received his medical degree from New York College and a Bachelor of Arts degree from New York University and has held hospital-based teaching positions. He has been sought after to teach physicians new clinical techniques worldwide for over 20 years. Dr. Victor has also been featured in international and local media as an expert in regenerative medicine, medical aesthetics and dermatology. Leonard Mazur, Chief Operating Officer Mr. Mazur also serves as an independent Board of Director and is presently the COO of Akrimax Pharma and former COO of Trimaz Pharma. He was CEO of Genesis Pharma sold to Pierre Fabre. At Medicus Pharma he was Ex VP of Sales and Marketing Anna Rhodes, Executive VP Operations Ms. Rhodes has been actively involved in the cosmetic and cosmeceuticals industries for over 9 years. From 2001 through 2009, Ms. Rhodes held various executive sales and marketing positions with Victor Cosmeceuticals, Inc. and Victor Products Inc., developing marketing and collateral materials, formulations and training materials for new product launches as well as managing domestic and international distribution. Prior to 2001, Ms. Rhodes held corporate executive managerial and sales positions in the high fashion industry with companies including Calvin Klein, Alberta Ferretti, Michael Kors and Agnona. She was a Magnum Cum Laude graduate of the University of Texas with a Bachelor of Science degree in Business Administration. Management (cont.) Anna Rhodes, Executive VP Operations Ms. Rhodes has been actively involved in the cosmetic and cosmeceuticals industries for over 9 years. From 2001 through 2009, Ms. Rhodes held various executive sales and marketing positions with Victor Cosmeceuticals, Inc. and Victor Products Inc., developing marketing and collateral materials, formulations and training materials for new product launches as well as managing domestic and international distribution. Prior to 2001, Ms. Rhodes held corporate executive managerial and sales positions in the high fashion industry with companies including Calvin Klein, Alberta Ferretti, Michael Kors and Agnona. She was a Magnum Cum Laude graduate of the University of Texas with a Bachelor of Science degree in Business Administration. 35 Board of Advisors Dr J ames Andrews, Sports Orthopedics Andrews Institute for Sports Medicine Dr J oshua Hackel, Andrews Sports Medicine Center, Florida Dr Sydney Coleman, Plastic Surgeon, New York Dr Greg Cavaliere, Orthopedic Surgeon, NY Rangers Dr Anthony Maddalo, Orthopedic Surgeon, NY Rangers Dr Nicholas Toscano, Periodontitis, Editor in Chief J IAD Dr Peter Bruno, Internist, New York City Fred Frank Vice-Chairman PJ Solmon, former Merrill Lynch healthcare banker J ack Schneider, former President Allen & Co. Dr Eric Richter, Neurologist, Chief LSU 36 Board of Directors Dr Steven Victor, Chairman & CEO, IntelliCell BioSciences Leonard Mazur, COO Triax, former EVP Sales & Marketing, Medicis Michael Hershman, Founder and CEO the Fairfax Group Myron Houbliak, former President Roche Therapeutics Inc. Sam Khashman, CEO of Imagine Technologies 37 Scientific Advisory Board (SAB) To assist the company in its clinical development programs, IntelliCell has assembled a scientific advisory board consisting of world-renowned researchers and experts in the field of Regenerative Medicine: Professor J oachim Kohn (Rutgers University) Professor J on Dobson (University of Florida) Professor J ared Bushman (Rutgers University) Professor Laith J azrawi (New York University) Subject Matter Specialists Biologics Consulting Group Andra E. Miller Ph.D. - Senior Consultant, Director Cell and Gene Therapies. 9 years experience as a molecular biologist and product reviewer with the FDA. Stephen Rhodes M.S. - Senior Consultant. Over 20 years of management experience with the FDA Center for Devices and Radiological Health. Holly Scott - Senior Consultant. 20 years of multi-office compliance experience with the FDA, including 4 years as a Consumer Safety Officer with FDA/CBER, and 15 years as a Field Investigator with the FDA Office of Regulatory Affairs/ Florida District Office. Buchanan Ingersoll & Rooney, PC Edward John Allera focuses on the development of new products and business opportunities in the areas of pharmaceuticals and technology, especially regarding the regulation and promotion of drugs, biologics and devices. Theodore M. Sullivan counsels clients subject to FDA regulations, advising in matters related to over-the-counter drug regulation, drug exclusivity issues, food and dietary supplement labeling and advertising and import detention of FDA-regulated products. 38