Biedermann Motech GmbH & Co. KG
Country not established
- Devices
- 1,297
What Biedermann Motech GmbH & Co. KG makes
Biedermann Motech produces spinal fixation systems, including pedicle screw assemblies and interbody devices designed for surgical stabilization of the spine. Their offerings include modular screw systems for posterior fixation and interbody cages for anterior support, primarily for lumbar and thoracic applications.
The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. These products are listed in the FDA’s 510(k) registry, reflecting their compliance with US medical device standards.
Catalogue
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Company details
- DUNS number
- 320249162
Frequently asked questions
How many devices does Biedermann Motech GmbH & Co. KG have in the registry?
The registry currently lists 1297 devices for Biedermann Motech GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biedermann Motech GmbH & Co. KG's devices?
Among its 50 most recently registered devices, Biedermann Motech GmbH & Co. KG has devices listed in EUDAMED (44 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Biedermann Motech GmbH & Co. KG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Biedermann Motech GmbH & Co. KG's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biedermann Motech GmbH & Co. KG in the registry?
The most recently registered devices listed for Biedermann Motech GmbH & Co. KG include NA 210-040-0740, NA 108-021-0045, NA 107-018-5060 and NA 108-018-4350.