Stephen A. Dunn, Inc. is one of 9805 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stephen A. Dunn, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POLYVUE, SILVER CHORD AND UNISOFT (METHAFILCON A) SPHERICAL, ASPHERICAL, TORIC AND MULTIFOCAL HYDROPHILIC CONTACT LENSE), DAILY WEAR SOFT (HYDROPHILIC) CONTACT LENS
2
Total
2
Cleared
0
Denied
Stephen A. Dunn, Inc. has 2 FDA 510(k) cleared medical devices. Based in Honolulu, US.
Historical record: 2 cleared submissions from 1996 to 1998. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Stephen A. Dunn, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stephen A. Dunn, Inc.
2 devices