Smt Schilling Metalltechnik GmbH
GermanyFDA applicant, unverified FDA FEI 3001026312
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Smt Schilling Metalltechnik GmbH makes
Smt Schilling Metalltechnik GmbH manufactures orthopedic guide wires and Kirschner wires, which are used in surgical procedures for bone alignment and fixation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Kirschner And Guide Wires Ref K100736
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3001026312
- Address
- GRIES WEG 33, MUHLHEIM Baden-Wurttemberg
Frequently asked questions
How many devices does Smt Schilling Metalltechnik GmbH have in the registry?
The registry currently lists 1 device for Smt Schilling Metalltechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smt Schilling Metalltechnik GmbH's devices?
Among its 1 most recently registered device, Smt Schilling Metalltechnik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Smt Schilling Metalltechnik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Smt Schilling Metalltechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smt Schilling Metalltechnik GmbH in the registry?
The most recently registered devices listed for Smt Schilling Metalltechnik GmbH include KIRSCHNER AND GUIDE WIRES.