FDA applicant

Phoenix Dental, Inc.

Fenton, MI5 decisions1994–20120 recalls

FDA records 5 decisions for Phoenix Dental, Inc. (Fenton, MI) from 1994 to 2012: 5 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and EJK (Liner, Cavity, Calcium Hydroxide). 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 Phoenix Dental, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Phoenix Dental, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Phoenix”

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

Phoenix Diagnostics, Inc. 21 Phoenix Biomedical Corp. 13 Phoenix Medical Technology, Inc. 11 Phoenix Glove Co. 6 Phoenix Bioengineering, Inc. 3 Phoenix Medical Devices, LLC 2 Phoenix Innovative Healthcare Manufacturers Pvt., Ltd. 2 Phoenix Biotech Corp. 2 Phoenix Imaging 2 Phoenix Surgical Products, Inc. 1 Phoenix Management, Inc. 1 Phoenix U.V.A., Ltd. 1

Phoenix Dental, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Phoenix”