Medical Device Manufacturer · US , Los Angeles , CA

Exelint International, Co. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2000

Total

Cleared

Denied

Exelint International, Co. has 7 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Latest FDA clearance: Dec 2025. Active since 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Exelint International, Co. Filter by specialty or product code using the sidebar.

Exelint International, Co. 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 - Exelint International, Co.

7 devices

1-7 of 7