Summary
Overview
Country or Region: USA
Industry: Manufacturing
NAICS: 423450
Company Profile:
IDL, Inc. brings great ideas to life through the design; manufacturing and distribution of Daily activity assist devices. Through problem-solving research and design, the Company seeks to develop innovative solutions to real needs in working, healing, learning, and living environments.
Benefits
- Recession Proof Market
- Massive Profit Margins
- 12K owned units in stock
- Large Dealer Margins
- Distributors added daily
- FDA registered
Order Fulfillment
- 24/7 Call Center
- 24 hour order processing
- Media Tracking
- Dealer Tracking
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IDL, Inc., (the “Company”) designs, creates and distributes Physical Medicine Therapeutic Devices a.k.a. Daily Activity Assist Devices for the world's disabled, elderly, and senior communities. The Company has developed an international reputation for being on the leading edge of assistive device design and integration. This technology focus and expertise has enabled the Company to take full advantage of the new generation of materials and manufacturing processes that combine life-long durability with professional quality injection molding systems using the Company’s patented designs.
The Company will develop and market medical devices through multiple distribution channels both foreign and domestic. The Company is currently developing its patent-applied technologies to final product and approval stage. It is also seeking to establish its corporate identity in the medical products field. Growth strategy calls for one joint venture license as well as the following objectives:
- Complete the patent process.
- Establish corporate identity, brand names, and trademarks.
- Establish a medical advisory board.
- Build staff, infrastructure, and retain dealers for sales and marketing.
- Complete GSA and Minority certifications.
- Continue R & D and product development.
- Explore options for 2nd round financing (venture capital, corporate alliance, licensing, and public offering) to maximize value to shareholders.
Note: Management believes that accelerated FDA approval process will be available on all the devices since our devices fall under a listing of medical devices exempt from 510(k) and Good Manufacturing Practices (GMP) compiled from Title 21 Code of Federal Regulations (CFR) and recent federal register.
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