Zyga Technology, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 47
What Zyga Technology, Inc. makes
Zyga Technology, Inc. manufactures the Simmetry Sacroiliac Joint Fusion System, a device designed for sacroiliac joint fusion procedures. This system is intended to stabilize the sacroiliac joint through surgical intervention, providing a solution for chronic sacroiliac joint pain or dysfunction.
The Simmetry Sacroiliac Joint Fusion System is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 47 devicesCompany details
- DUNS number
- 024049072
Frequently asked questions
How many devices does Zyga Technology, Inc. have in the registry?
The registry currently lists 47 devices for Zyga Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zyga Technology, Inc.'s devices?
Among its 47 most recently registered devices, Zyga Technology, Inc. has devices listed in FDA 510(k) (6 devices) and FDA GUDID (41 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Zyga Technology, Inc.'s devices fall under?
Among its 47 most recently registered devices, the classes recorded for Zyga Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zyga Technology, Inc. in the registry?
The most recently registered devices listed for Zyga Technology, Inc. include SImmetry® 10-S10570-01, SImmetry® 10-P14550-01, SImmetry® 10-S08590-01 and SImmetry® 10-P14555-01.