Seidel Medizin GmbH
Country not established
- Devices
- 2
What Seidel Medizin GmbH makes
Seidel Medizin GmbH manufactures the Larkel device, including its variants with attachments labeled A-H and a modified version of the same. These devices are designed for medical procedures requiring secure tissue attachment or stabilization.
The Larkel device and its modifications are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Larkel Device W/Attachments A-H Ref K872486
Regimes: 510(k) Registry: 510(k)Larkel Device With Attachments A-H(Modification) Ref K953559
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seidel Medizin GmbH have in the registry?
The registry currently lists 2 devices for Seidel Medizin GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seidel Medizin GmbH's devices?
Among its 2 most recently registered devices, Seidel Medizin GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Seidel Medizin GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Seidel Medizin GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seidel Medizin GmbH in the registry?
The most recently registered devices listed for Seidel Medizin GmbH include LARKEL DEVICE W/ATTACHMENTS A-H and LARKEL DEVICE WITH ATTACHMENTS A-H(MODIFICATION).