Medix, Inc. is one of 24545 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PROTECTIV JELCO SAFETY I.V. CATHETER, MODEL 3600 SERIES
1
Total
1
Cleared
0
Denied
Medix, Inc. is a healthcare staffing and workforce solutions provider based in Dublin, US. The company specializes in recruiting and placing skilled professionals across healthcare, life sciences, and technology sectors.
Medix, Inc. has received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory activity focused on General Hospital devices, with clearance granted in 2004. The company is inactive in the FDA 510(k) database, with no submissions recorded in more than 5 years, and should be treated as a historical regulatory record.
The cleared device on record is the PROTECTIV JELCO SAFETY I.V. CATHETER, MODEL 3600 SERIES, a General Hospital device. For detailed information on device names, product codes, and clearance dates, review the company's complete 510(k) submission history.
FDA 510(k) Regulatory Record - Medix, Inc.
1 devices