Medical Device Manufacturer · US , Mchenry , IL

Cederroth, Inc. USA - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 1982

Total

Cleared

Denied

Cederroth, Inc. USA has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 6 cleared submissions from 1982 to 1988. Primary specialty: General & Plastic Surgery.

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

Cederroth, Inc. USA 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 - Cederroth, Inc. USA

7 devices

1-7 of 7