Medical Device Manufacturer · US , Mchenry , IL

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

7 submissions · 7 cleared · Since 1981

Total

Cleared

Denied

Lada Intl., Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1981 to 1988. Primary specialty: General & Plastic Surgery.

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

Lada 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 - Lada Intl., Inc.

7 devices

1-7 of 7