FDA applicant

Suncoast Dental, Inc. Dba Tatum Surgical

Clearwater, FL1 decision2022–20220 recalls

FDA records 1 decision for Suncoast Dental, Inc. Dba Tatum Surgical (Clearwater, FL) in 2022: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 13 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 Suncoast Dental, Inc. Dba Tatum Surgical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Suncoast Dental, Inc. Dba Tatum Surgical by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Suncoast Dental, Inc. Dba Tatum Surgical’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 “Suncoast”

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

Suncoast Medical Manufacturers, Inc. 31 Suncoast Dental Corp. 2 Suncoast Medical Products, Inc. 1

Suncoast Dental, Inc. Dba Tatum Surgical

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 “Suncoast”