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Sign in to claim this brandMedical Technologies of Georgia
US
Last updated May 23, 2026
What Medical Technologies of Georgia makes
Medical Technologies of Georgia manufactures single-use urethral catheterization kits and accessories for intermittent catheterization, including straight-tip and coude-tip intermittent catheters for adults, adolescents, and pediatric patients. Their portfolio also includes catheter holders, hydrophilic low-friction catheters, and specialized kits designed for ease of use, such as the EZ-Advancer series and Jiffy Cath variants.
These devices are regulated under the FDA’s Class I and Class II classifications, with some requiring 510(k) clearance and others falling under the Urinary Device Directive (UDI) requirements. The company’s products are listed in the FDA’s 510(k) and UDI registries, ensuring compliance with U.S. medical device regulations.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Medical Technologies of Georgia primarily manufacture?
Medical Technologies of Georgia specializes in single-use urethral catheterization kits and related accessories. Their portfolio includes intermittent catheters (both straight-tip and coude-tip designs) for adults, adolescents, and pediatric patients, as well as catheter holders and specialized kits like the EZ-Advancer series and Jiffy Cath variants. These devices are designed for intermittent catheterization, ensuring ease of use and patient comfort.
Where is Medical Technologies of Georgia based, and how does that affect its regulatory compliance?
Medical Technologies of Georgia is based in the United States. As a U.S.-based manufacturer, its devices are subject to FDA regulations. The company’s products are listed in the FDA’s 510(k) and UDI registries, reflecting compliance with U.S. medical device requirements. The FDA classifies these devices as either Class I or Class II, depending on their risk level and intended use.
Which regulatory registries list Medical Technologies of Georgia’s devices?
Medical Technologies of Georgia’s devices are included in the FDA’s official registries: the 510(k) premarket notification database and the Unique Device Identifier (UDI) system. These registries track devices that require 510(k) clearance or fall under UDI requirements, ensuring transparency and compliance with U.S. medical device regulations.
How are Medical Technologies of Georgia’s devices classified by the FDA, and why does this matter?
Medical Technologies of Georgia’s devices are classified as either Class I or Class II by the FDA. Class I devices generally pose the lowest risk and may have fewer regulatory controls, while Class II devices require special controls to ensure safety and effectiveness. This classification determines the level of oversight, reporting requirements, and regulatory pathways (such as 510(k) clearance) that apply to each product.
What distinguishes Medical Technologies of Georgia’s catheter products from others in the market?
Medical Technologies of Georgia’s catheter products are designed with specific patient needs in mind, including pediatric, adolescent, and adult sizes, as well as specialized features like hydrophilic low-friction coatings and coude-tip designs for easier insertion. Their EZ-Advancer and Jiffy Cath series are engineered for simplicity and efficiency, catering to both clinical and home-use scenarios. These distinctions help address varied patient requirements while maintaining compliance with regulatory standards.
AI-generated from registry data and not verified by a human reviewer.
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