Bennett Jacoby, Dds, Ms, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bennett Jacoby, Dds, Ms, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip
1
Total
1
Cleared
0
Denied
Bennett Jacoby, Dds, Ms, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kailua Kona, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bennett Jacoby, Dds, Ms, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Contract In-House Counsel & Consultants, LLC (D/B/A FDA Atty as regulatory consultant.
FDA 510(k) Regulatory Record - Bennett Jacoby, Dds, Ms, Inc.
1 devices