Gorsk, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Gorsk, Inc. makes
Gorsk, Inc. manufactures medical instruments and containment systems, including the Gorsk Instrument Rest and the Gorsk Sponge Containment System, designed for surgical and procedural use.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Gorsk Instrument Rest Ref K873554
Regimes: 510(k) Registry: 510(k)Gorsk Sponge Containment System Ref K873555
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gorsk, Inc. have in the registry?
The registry currently lists 2 devices for Gorsk, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gorsk, Inc.'s devices?
Among its 2 most recently registered devices, Gorsk, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gorsk, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gorsk, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gorsk, Inc. in the registry?
The most recently registered devices listed for Gorsk, Inc. include GORSK INSTRUMENT REST and GORSK SPONGE CONTAINMENT SYSTEM.