Cresco TI Systems AB
Country not established
- Devices
- 2
What Cresco TI Systems AB makes
Cresco TI Systems AB manufactures the Cresco TI Implant Concept, a medical device designed for transcutaneous implantation, including modifications to the original implant design. These devices are intended for specific surgical applications requiring internal fixation or stabilization.
The Cresco TI Implant Concept is classified as a Class II medical device under FDA regulations and is supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Modification To: Cresco Ti Implant Concept Ref K042354
510(k) 510(k)Cresco Ti Implant Concept Ref K981052
510(k) 510(k)
Frequently asked questions
How many devices does Cresco TI Systems AB have in the registry?
The registry currently lists 2 devices for Cresco TI Systems AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cresco TI Systems AB's devices?
Among its 2 most recently registered devices, Cresco TI Systems AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Cresco TI Systems AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cresco TI Systems AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cresco TI Systems AB in the registry?
The most recently registered devices listed for Cresco TI Systems AB include MODIFICATION TO: CRESCO TI IMPLANT CONCEPT and CRESCO TI IMPLANT CONCEPT.