510(k) Report

FDA applicant

Deepak Products, Inc.

Miami, FL1 decision2004–20040 recalls

FDA records 1 decision for Deepak Products, Inc. (Miami, FL) in 2004: 1 510(k) clearance. All are in product code EJR (Agent, Polishing, Abrasive, Oral Cavity). 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 Deepak Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Deepak Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Deepak Products, 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