Profile: Dreve Otoplastik GmbH provides dental and hearing care products. We are accredited with ISO 9001:2000 certification. We manufacture earmoulds under the brand name of FotoTec® using stereolithography. We provide an online shopping to the customers. The earmould is the connection between ear and hearing system. Our FotoTec® lifestyle earmould works with the open fitting technology. It is manufactured in the stereolithography process. The modern manufacturing process guarantees a perfect fitting & makes an innovative design. Our ear impression products include otoform® which has the excellent scanning characteristics for the fortec® process. Our hygiene product reacts with antimicrobial agent offers advanced protection against bacteria & fungus.
The company has ~130 employees and is ISO 9001, CE certified.
FDA Registration Number: 3003610251
US Agent: Mike Kollar / Dreve America Corp.
Phone: +1-(612)-323-8803 E-Mail:
17 Products/Services (Click for related suppliers)
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• Air Conduction Hearing Aid (FDA Code: ESD / 874.3300) A hearing aid is wearable sound-amplifying device that is intended to compensate for impaired hearing. This generic type of device includes the air-conduction hearing aid and the bone-conduction hearing aid, but excludes the group hearing aid or group auditory trainer (874.3320), master hearing aid (874.3330), and tinnitus masker (874.3400). |
• Disinfection Spray |
• Earmold |
• Fiber Optic Otoscopes |
• Hand Cleaner Gel |
• Hearing Aids |
• Insert Hearing Protector (FDA Code: EWD) |
• 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 Otoscopes |
• Medical Tweezer |
• Otoscope Aids |
• Silicon Elastomer ENT Synthetic-PIFE Polymer (FDA Code: ESH / 874.3620) Ear, nose, and throat synthetic polymer material is a device material that is intended to be implanted for use as a space-occupying substance in the reconstructive surgery of the head and neck. The device is used, for example, in augmentation rhinoplasty and in tissue defect closures in the esophagus. The device is shaped and formed by the suregon to conform to the patient's needs. This generic type of device is made of material such as polyamide mesh or foil and porous polyethylene. |
• Silicone Component |
• Silicone Rubber Elastomer |
• Skin Protective Supportive Moldable Orthosis (FDA Code: MNE / 890.3475) |
• Tweezers |
• Ultraviolet Polymerization Chamber |