GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH
Medical Technology · Mannheim
GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH is a medical technology company based in Mannheim, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).
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GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH Address & Contact
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GEIß & NIEDERSETZ ZAHNTECHNIK GMBH Overview
GEIß & NIEDERSETZ ZAHNTECHNIK GMBH from Mannheim in Baden-Württemberg is a renowned dental laboratory that has established itself in the Rhine-Neckar metropolitan region. The laboratory specializes in the production of dental prosthetics, crowns, bridges, and implant superstructures, serving local dental practices in the Mannheim-Heidelberg-Ludwigshafen region. Mannheim, as the third largest city in Baden-Württemberg, plays a central role in the healthcare industry and has positioned itself as an important location for medical technology and dentistry. With a strong local infrastructure and well-trained professionals, the company offers high-quality products and services.
Services and Products
GEIß & NIEDERSETZ offers a comprehensive range of dental prosthetic solutions. Prosthetics are manufactured in a variety of materials, including:
- All-ceramic: Ideal for aesthetic reconstructions, as it provides excellent light permeability.
- Zirconia: Particularly durable and stable, often used for implant crowns.
- Metal-ceramic composite materials: A combination of metal and ceramics ensures high stability and natural aesthetics.
- Removable dental prosthetics: Provides patients with a cost-effective solution for gaps in their teeth.
The laboratory utilizes modern CAD/CAM milling technology and digital workflows to develop customized solutions for the individual needs of patients. By implementing digital workflows, not only is precision increased, but processing times are significantly reduced. The customer base includes not only dental practices but also specialized implantologists who rely on high-quality and precisely fitting solutions.
Regulatory Classification
As a provider of medical devices, GEIß & NIEDERSETZ is subject to strict regulatory requirements in accordance with the EU Medical Devices Regulation (MDR). All products must undergo comprehensive quality checks to ensure safety and effectiveness. The dental laboratory conducts regular internal audits and adheres to current quality standards to maintain certifications according to ISO 13485. This ensures that all production processes meet the highest standards and that the products comply with legal regulations.
Location Mannheim / Baden-Württemberg
Mannheim has emerged as a significant location for the healthcare sector in Germany. The proximity to numerous hospitals, specialist centers, and educational institutions such as the University of Mannheim makes the city an attractive environment for innovative companies in the field of medical technology. Furthermore, the Rhine-Neckar metropolitan region, with its strong network of science and industry, offers numerous cooperation opportunities and a lively exchange between research and practice.
In addition to its direct regional significance, GEIß & NIEDERSETZ also influences the national health system. Through close collaboration with dentists and clinics, the laboratory contributes to the improvement of dental care and thus enables efficient treatment of patients throughout the country.
Moreover, GEIß & NIEDERSETZ is committed to the further education of professionals and offers training on modern technologies in dentistry. This not only promotes the development of employees but also helps dental practices stay up to date with the latest advancements.
More medical technology companies: Medical Technology Overview | Laboratories | Pharmaceutical Companies
```Frequently asked questions about GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH
What does GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH do?
GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH is a company in the medical technology sector based in Mannheim. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.
Where is GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH located?
GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH is headquartered in Mannheim. More information can be found on the company's website.
In which area of medical technology is GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH active?
GEIß & NIEDeutschlandRSETZ ZAHNTECHNIK GMBH is active in the medical technology sector and offers solutions for medical facilities, clinics and practices. You can find the exact areas of focus on the company's website.
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About Medical Technology
Germany's medical technology sector is one of the most important in the world. With annual revenues of approximately EUR 36 billion and more than 1,400 companies, Germany ranks as the third-largest medical technology market globally (SPECTARIS 2023), after the United States and Japan. The sector encompasses the development, manufacture and distribution of an extraordinarily wide range of products: in-vitro diagnostic (IVD) devices, medical imaging systems (CT, MRI, ultrasound), implants such as hip and knee prostheses, cardiac pacemakers, surgical instruments, hospital beds, wound care products and medical software classified as a Software as a Medical Device (SaMD). In Germany and across the European Union, medical devices must comply with the EU Medical Device Regulation (MDR 2017/745), which replaced the former Medical Devices Directive (MDD 93/42/EEC). Devices are classified into risk classes I, IIa, IIb and III. Higher-risk classes require a conformity assessment by a designated Notified Body (benannte Stelle) before a CE mark can be affixed. The CE mark signals that the product meets EU safety, performance and quality requirements and may be placed on the European market. Key medtech clusters in Germany include the Munich and Nuremberg region in Bavaria, the Rhine-Main area in Hesse, Tuttlingen in Baden-Württemberg (known as the world capital of surgical instruments) and the Hamburg metropolitan area. This directory lists CE-certified manufacturers, distributors and suppliers across the German medtech sector with full contact details.
Germany as a Global Medical Technology Hub
Germany's position as the world's third-largest medical technology market is underpinned by a combination of industrial engineering excellence, a well-funded healthcare system and a highly productive research landscape. The German medtech sector is characterised by a large number of small and medium-sized enterprises (SMEs) that are often hidden champions (Weltmarktführer) in specialised niches. Unlike the pharmaceutical sector, where large corporations dominate, the medtech industry is more fragmented and innovative, with frequent spin-offs from university hospitals and engineering faculties. Key product categories include imaging systems (MRI, CT, X-ray, ultrasound), endoscopy and minimally invasive surgical tools, orthopaedic implants, cardiovascular devices, in-vitro diagnostics, dental equipment, ophthalmic devices, wound care systems and hospital IT and medical software. Germany is particularly renowned for its surgical instrument manufacturing, centred in Tuttlingen, Baden-Württemberg, which supplies operating theatres worldwide. The annual Medica trade fair in Düsseldorf is the world's largest medical technology exhibition and serves as a global industry showcase.
EU MDR Compliance and CE Marking for German Manufacturers
The EU Medical Device Regulation (MDR 2017/745) replaced the former Medical Devices Directive (MDD 93/42/EEC) and has applied in full since May 2021, with transition periods for legacy devices extended to 2028 in some cases. For German manufacturers selling in the EU market, MDR compliance is a legal necessity. The regulation introduced significantly strengthened requirements compared to the old MDD: more rigorous clinical evidence requirements, mandatory post-market clinical follow-up (PMCF), unique device identification (UDI) registration in the EUDAMED database, increased obligations for Notified Bodies, and stricter rules for software as a medical device (SaMD). The risk classification system under MDR uses four classes (I, IIa, IIb, III) based on the intended purpose, duration of use and body contact of the device. Manufacturers must appoint an authorised representative in the EU if they are not themselves based in an EU member state, and they must maintain a quality management system. In Germany, the Bundesnetzagentur and state authorities support MDR enforcement alongside BfArM.
Innovation and Research in German Medtech
Germany's medtech innovation ecosystem benefits from close collaboration between industry, university hospitals (Universitätsklinika), applied research institutes (such as those of the Fraunhofer and Helmholtz networks) and health technology assessment bodies. The Federal Joint Committee (Gemeinsamer Bundesausschuss, G-BA) and the Institute for Quality and Efficiency in Health Care (Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen, IQWiG) play important roles in assessing which new medical technologies are eligible for reimbursement by statutory health insurance (GKV). This reimbursement pathway, known as the NUB process (Neue Untersuchungs- und Behandlungsmethoden) for hospital technologies, is a key milestone for commercial success in Germany. Innovative devices that receive a positive NUB assessment can be reimbursed at negotiated rates by statutory insurers, providing a significant market access advantage.
Innovation Fields and Future Technologies
The German medical technology sector is driving numerous future fields forward. AI-supported diagnostics and image analysis are revolutionising radiology and pathology; algorithms for the early detection of cancer and cardiovascular disease are increasingly receiving CE approvals as Software as a Medical Device (SaMD). Robot-assisted surgical systems, led by products from Siemens Healthineers, Brainlab and Karl Storz, are improving precision in complex procedures. Minimally invasive technologies, implantable pacemakers and intelligent prostheses with sensory feedback demonstrate the breadth of innovation. Point-of-care diagnostics enables rapid tests directly in the doctor's surgery or at the bedside. Telemedicine and digital patient records promote networking between medical devices and clinical workflows. The Federal Ministry of Education and Research (BMBF) funding programme specifically supports the development of innovative medical technology products through cooperation between industry and universities.
What does the medical technology sector cover?
Medical technology encompasses the development, manufacture and distribution of medical devices, instruments, software and accessories used to diagnose, prevent, monitor or treat diseases. Germany ranks among the world's leading medical technology hubs.
How are medical devices approved in Germany?
Medical devices in Germany and the EU must comply with the EU Medical Device Regulation (MDR 2017/745) and carry the CE mark. Depending on the risk class, conformity assessments by notified bodies are required.
Where can I find medical technology companies in Germany?
Medical technology companies in Germany can be found through industry associations such as SPECTARIS, BVMed or ZVEI, and via the EUDAMED EU database for registered manufacturers. Sanoliste provides a searchable directory of manufacturers, distributors and suppliers across the German medical technology sector.
How many medical technology companies are there in Germany?
Germany has more than 1,400 medical technology companies generating annual revenues of approximately EUR 36 billion (SPECTARIS 2023), making it the third-largest medical technology market in the world. The majority of companies are small and medium-sized enterprises (SMEs), many of which are world market leaders in their niche.
What are the risk classes for medical devices under the EU MDR?
The EU Medical Device Regulation (MDR 2017/745) classifies medical devices into four risk classes: Class I (lowest risk, e.g. bandages, glasses frames), Class IIa (medium risk, e.g. hearing aids, contact lenses), Class IIb (higher medium risk, e.g. infusion pumps, ventilators) and Class III (highest risk, e.g. implantable cardiac devices, neurosurgical instruments). Higher classes require more rigorous conformity assessment by a Notified Body.
Where are the main medical technology clusters in Germany?
Germany's medical technology industry is concentrated in several regional clusters. Bavaria (particularly Munich and Nuremberg) and Baden-Württemberg (notably Tuttlingen, globally known for surgical instruments) are the two strongest regions. Other significant clusters include the Rhine-Main area in Hesse, the Hamburg metropolitan region, the Ruhr area in North Rhine-Westphalia and the Berlin-Brandenburg region.
What is a Notified Body (benannte Stelle) and why does it matter?
A Notified Body (benannte Stelle) is an independent third-party organisation designated by an EU member state to assess whether medical devices meet the requirements of the MDR before they can carry the CE mark. For Class IIa, IIb and III devices, manufacturers must have their quality management system and technical documentation assessed by a Notified Body. In Germany, the Federal Institute for Drugs and Medical Devices (BfArM) oversees market surveillance, while several German organisations hold Notified Body status under the MDR.