FDA applicant

Protech Professional Products, Inc.

Centereach, NY2 decisions1993–20150 recalls

FDA records 2 decisions for Protech Professional Products, Inc. (Centereach, NY) from 1993 to 2015: 2 510(k) clearances. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). 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 Protech Professional Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Protech”

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

Protech Products 1 Protech, Inc. 1 Protech Industries Co., Ltd. 1

Protech Professional Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Protech”