510(k) Report

FDA applicant

Bud Industries, Inc.

Holland, NY3 decisions1991–19950 recalls

FDA records 3 decisions for Bud Industries, Inc. (Holland, NY) from 1991 to 1995: 3 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and JEY (Plate, Bone). 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 Bud Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bud Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bud Industries, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DZEImplant, Endosseous, Root-Form2decisions
  • JEYPlate, Bone1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K912521Dental Implant System 4.0MM and 5.5MM LengthBud Industries, Inc. · 19951cites it

What has FDA decided for it lately?

  • K912521Dental Implant System 4.0MM and 5.5MM LengthBud Industries, Inc. · 1995
  • K913688Bud Maxillofacial Implant SystemBud Industries, Inc. · 1992
  • K902331Bud Dental Implant SystemBud Industries, Inc. · 1991

All 3 as Bud Industries, Inc. →