Coil is one of 7141 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Coil, is a medical device manufacturer with a manufacturing facility in Baltimore, US. The company specializes in ophthalmic devices and has maintained an FDA registered facility for medical device production.
Coil received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory activity occurred in 1997, with the clearance of PATHFINDER SUNGLASSES, an ophthalmic device. Coil is currently inactive with no FDA submissions recorded in the past 25 years, and this profile serves as a historical regulatory record.
For detailed information on cleared device names, product codes, and clearance dates, please review the complete 510(k) submission history.
FDA 510(k) Regulatory Record - Coil
1 devices