FDA applicant

Janco Polymers Pvt., Ltd.

India, IN1 decision1990–19900 recalls

FDA records 1 decision for Janco Polymers Pvt., Ltd. (India, IN) in 1990: 1 510(k) clearance. All are in product code 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, general hospital panel, where it files most

How often FDA has decided Janco Polymers Pvt., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Janco Polymers Pvt., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Janco Polymers 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 “Janco”

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

Janco Consulting Services 3

Janco Polymers Pvt., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Janco”