FDA applicant

Frontline Latex Products Pvt., Ltd.

New York, NY2 decisions1989–19960 recalls

FDA records 2 decisions for Frontline Latex Products Pvt., Ltd. (New York, NY) from 1989 to 1996: 2 510(k) clearances. Most are in product codes HIS (Condom) and LYY (Latex Patient Examination Glove). 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 Frontline Latex Products Pvt., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Frontline Latex Products Pvt., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Frontline”

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

Frontline Medical 2

Frontline Latex Products Pvt., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Frontline”