Dilling Co.
Country not established
- Devices
- 1
What Dilling Co. makes
Dilling Co. manufactures the Gerbode sternal retractor, a surgical instrument designed to provide exposure during sternal procedures by holding the sternum apart.
The company’s portfolio is regulated under FDA Class II devices, with the Gerbode sternal retractor authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Retractor, Gerbode Sternal Ref K760650
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dilling Co. have in the registry?
The registry currently lists 1 device for Dilling Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dilling Co.'s devices?
Among its 1 most recently registered device, Dilling Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Dilling Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dilling Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dilling Co. in the registry?
The most recently registered devices listed for Dilling Co. include RETRACTOR, GERBODE STERNAL.