Hartmann Group, Inc.
Country not established
- Devices
- 1
What Hartmann Group, Inc. makes
Hartmann Group, Inc. manufactures automated suture forceps, designed for precise tissue approximation and closure in surgical procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Forceps, Suture, Auto Ref K772286
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hartmann Group, Inc. have in the registry?
The registry currently lists 1 device for Hartmann Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hartmann Group, Inc.'s devices?
Among its 1 most recently registered device, Hartmann Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hartmann Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hartmann Group, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hartmann Group, Inc. in the registry?
The most recently registered devices listed for Hartmann Group, Inc. include FORCEPS, SUTURE, AUTO.