Axis is one of 10804 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Axis - FDA 510(k) Cleared Devices
Recent clearances: AXIS %CDT TURBIDIMETRIC IMMUNOASSAY
1
Total
1
Cleared
0
Denied
Axis, is a medical device manufacturer with a registered facility in San Diego, US. The company specializes in Chemistry devices for clinical laboratory applications.
Axis has received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory activity spans from 1999 to 1999, with its cleared device in the Chemistry category. Axis is currently inactive, with no FDA clearances recorded in more than five years, and should be treated as a historical record.
The company's cleared device includes the AXIS %CDT TURBIDIMETRIC IMMUNOASSAY, a Chemistry-based diagnostic system. Explore the device name, product codes, and clearance dates in the full regulatory database.
FDA 510(k) Regulatory Record - Axis
1 devices