Zygofix Ltd
IsraelFDA 510(k) applicant, unverified
- Devices
- 15
What Zygofix Ltd makes
ZygoFix Ltd manufactures non‑bioabsorbable spinal bone screws for use in spinal fixation procedures. Their product line includes a range of zLOCK screws in sizes from 1.5 mm to 4.0 mm, as well as facet screws and assorted tool trays (e.g., Tray #1, Tray #2, Tray #3, and combined trays). These devices are intended for implantation in the vertebral column to provide stable fixation during surgical reconstruction.
The spinal screw portfolio is classified as Class U devices and is listed in the FDA 510(k) database and the FDA Unique Device Identification (UDI) system. ZygoFix Ltd is based in the United States.
Catalogue
Search and filter all 15 devicesCompany details
- DUNS number
- 532143561
Frequently asked questions
How many devices does ZYGOFIX LTD have in the registry?
The registry currently lists 15 devices for ZYGOFIX LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list ZYGOFIX LTD's devices?
Among its 15 most recently registered devices, ZYGOFIX LTD has devices listed in FDA 510(k) (2 devices) and FDA GUDID (13 devices). A device can be listed in more than one registry, so these counts overlap.
What are the newest devices from ZYGOFIX LTD in the registry?
The most recently registered devices listed for ZYGOFIX LTD include Facet screw 1, zLOCK tools Tray #1, zLOCK tools Tray #3 1 and zLOCK 3.0mm.