Medical Device Manufacturer · CA , Brantford Ontario

Germiphene Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1989

Total

Cleared

Denied

Germiphene Corp. has 5 FDA 510(k) cleared medical devices. Based in Brantford Ontario, CA.

Historical record: 5 cleared submissions from 1989 to 1998. Primary specialty: Dental.

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

Germiphene Corp. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Germiphene Corp.

5 devices

1-5 of 5