Micomed GmbH
Country not established
- Devices
- 2
What Micomed GmbH makes
Micomed GmbH manufactures orthopedic instrumentation, including the Halm Zielke instrumentation for spinal and orthopedic surgical procedures, and the Posterior Doublerod System (MPDS), designed for spinal stabilization and fixation.
The company’s products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Micomed - Halm Zielke Instrumentation Ref K982006
Regimes: 510(k) Registry: 510(k)Micomed Posterior Doublerod System (Mpds) Ref K991862
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micomed GmbH have in the registry?
The registry currently lists 2 devices for Micomed GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micomed GmbH's devices?
Among its 2 most recently registered devices, Micomed GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Micomed GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Micomed GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micomed GmbH in the registry?
The most recently registered devices listed for Micomed GmbH include MICOMED - HALM ZIELKE INSTRUMENTATION and MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS).