510(k) Report

FDA applicant

Reddy Medtech Health Products, Ltd.

Plainsboro, NJ4 decisions1998–19980 recalls

FDA records 4 decisions for Reddy Medtech Health Products, Ltd. (Plainsboro, NJ) in 1998: 4 510(k) clearances. Most are in product codes LTZ (Condom With Nonoxynol-9) and HIS (Condom). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Reddy Medtech Health Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Reddy Medtech Health Products, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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