Medical Device Manufacturer · US , Mchenry , IL

Surgilite Intl., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1977

Total

Cleared

Denied

Surgilite Intl., Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 5 cleared submissions from 1977 to 1983. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Surgilite Intl., Inc. Filter by specialty or product code using the sidebar.

Surgilite Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Surgilite Intl., Inc.

5 devices

1-5 of 5