Hct, Inc.
Country not established
- Devices
- 1
What Hct, Inc. makes
Hct, Inc. manufactures the Villalta Retractor, a surgical instrument designed to provide stable retraction during procedures requiring clear visualization of anatomical structures.
The Villalta Retractor is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Villalta Retractor Ref K943875
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hct, Inc. have in the registry?
The registry currently lists 1 device for Hct, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hct, Inc.'s devices?
Among its 1 most recently registered device, Hct, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hct, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hct, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hct, Inc. in the registry?
The most recently registered devices listed for Hct, Inc. include VILLALTA RETRACTOR.