510(k) Report

FDA applicant

Bennett Jacoby, Dds, Ms, Inc.

Kailua Kona, HI1 decision2020–20200 recalls

FDA records 1 decision for Bennett Jacoby, Dds, Ms, Inc. (Kailua Kona, HI) in 2020: 1 510(k) clearance. All are in product code DZI (Drill, Bone, Powered). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Bennett Jacoby, Dds, Ms, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020: 1
2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Bennett Jacoby, Dds, Ms, Inc. by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DZIDrill, Bone, Powered1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K192033Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour…Bennett Jacoby, Dds, Ms, Inc. · 2020

The one decision as Bennett Jacoby, Dds, Ms, Inc. →

Other applicant names beginning “Bennett”

FDA records each applicant name separately; these may or may not be the same firm.

Bennett X-Ray Corp. 23Bennett X-Ray Technologies 2Bennett and Assoc., Inc. 1Bennett Ergonomic Labs, Inc. 1