Medical Device Manufacturer · US , Crofton , MD

Latexx Partners Bhd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1998

Total

Cleared

Denied

Latexx Partners Bhd. has 7 FDA 510(k) cleared medical devices. Based in Crofton, US.

Historical record: 7 cleared submissions from 1998 to 2001. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Latexx Partners Bhd. Filter by specialty or product code using the sidebar.

Latexx Partners Bhd. 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 - Latexx Partners Bhd.

7 devices

1-7 of 7