Canica Design, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Canica Design, Inc. makes
Canica Design, Inc. manufactures the CHESS Hand Surgery System, a device designed for minimally invasive surgical procedures in hand and wrist operations.
The CHESS Hand Surgery System is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Chess Hand Surgery System Ref K010184
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Canica Design, Inc. have in the registry?
The registry currently lists 1 device for Canica Design, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Canica Design, Inc.'s devices?
Among its 1 most recently registered device, Canica Design, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Canica Design, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Canica Design, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Canica Design, Inc. in the registry?
The most recently registered devices listed for Canica Design, Inc. include CHESS HAND SURGERY SYSTEM.