Profile: Young Dental Manufacturing Co. designs, manufactures & distributes consumable supplies, instruments & other products that are used by dental professionals primarily in preventive dentistry, restorative procedures and instrument sterilization. Our Kwick-EZ™ foam trays are comfortable for gel and foam application.
The company is ISO 9001, CE certified. NASDAQ:YDNT (SEC Filings)
FDA Registration Number: 1941138
15 Products/Services (Click for related suppliers)
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• Ammonia Inhalants |
• Aspirators |
• Cold Sterilization Solution |
• Cotton, Rayon Supplies |
• Dental Syringes |
• General Medical Supplies |
• Infection Control Systems |
• Inhalants |
• Medical Device, Sterilant (FDA Code: MED / 880.6885) A liquid chemical sterilant/high level disinfectant is a germicide that is intended for use as the terminal step in processing critical and semicritical medical devices prior to patient use. Critical devices make contact with normally sterile tissue or body spaces during use. Semicritical devices make contact during use with mucous membranes or nonintact skin. |
• Medical Devices, Disinfectant (FDA Code: LRJ / 880.6890) A general purpose disinfectant is a germicide intended to process noncritical medical devices and equipment surfaces. A general purpose disinfectant can be used to preclean or decontaminate critical or semicritical medical devices prior to terminal sterilization or high level disinfection. Noncritical medical devices make only topical contact with intact skin. |
• Medical Instrument Ultrasonic Cleaner (FDA Code: FLG / 880.6150) An ultrasonic cleaner for medical instruments is a device intended for cleaning medical instruments by the emission of high frequency soundwaves. |
• Physical/Chemical Sterilization Process Indicator (FDA Code: JOJ / 880.2800) A biological sterilization process indicator is a device intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor adequacy of sterilization. The device consists of a known number of microorganisms, of known resistance to the mode of sterilization, in or on a carrier and enclosed in a protective package. Subsequent growth or failure of the microorganisms to grow under suitable conditions indicates the adequacy of sterilization. |
• Sterilization Wrap (FDA Code: FRG / 880.6850) A sterilization wrap (pack, sterilization wrapper, bag, or accessories, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used. |
• Sterilization Wrap Containers (FDA Code: KCT / 880.6850) |
• Surgical Masks (FDA Code: FXX / 878.4040) Surgical apparel are devices that are intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate material. Examples include surgical caps, hoods, masks, gowns, operating room shoes and shoe covers, and isolation masks and gowns. Surgical suits and dresses, commonly known as scrub suits, are excluded. |