Dimeco is one of 25292 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dimeco - FDA 510(k) Cleared Devices
Recent clearances: CLINIC 2000 MODEL MULTI-FRECODYN DEVICE
1
Total
1
Cleared
0
Denied
Dime, co is a medical device company with a manufacturing facility in McHenry, US. The company has a historical record of FDA 510(k) submissions in the Physical Medicine device category.
Dimeco received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory activity dates to 1982, focusing exclusively on Physical Medicine devices. Dimeco is currently inactive with no clearances recorded in more than five years and should be treated as a historical regulatory record.
For detailed information on cleared device names, product codes, and clearance dates, review the company's complete 510(k) submission history.
FDA 510(k) Regulatory Record - Dimeco
1 devices