Medical Device Manufacturer · US , Sugar Land , TX

Quali-Med, Inc. - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 1986

Total

Cleared

Denied

Quali-Med, Inc. has 6 FDA 510(k) cleared medical devices. Based in Sugar Land, US.

Historical record: 6 cleared submissions from 1986 to 1987. Primary specialty: General & Plastic Surgery.

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

Quali-Med, 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 - Quali-Med, Inc.

7 devices

1-7 of 7