Medical Device Manufacturer · US , Miami Lakes , FL

Windmere Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1990

Total

Cleared

Denied

Windmere Corp. has 7 FDA 510(k) cleared medical devices. Based in Miami Lakes, US.

Historical record: 7 cleared submissions from 1990 to 1998. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Windmere Corp. Filter by specialty or product code using the sidebar.

Windmere Corp. 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 - Windmere Corp.

7 devices

1-7 of 7