510(k) Report

FDA applicant

Sri Anusham Rubber Industries Pvt., Ltd.

Vadasery, Nagercoil, Tn, IN6 decisions1992–19990 recalls

FDA records 6 decisions for Sri Anusham Rubber Industries Pvt., Ltd. (Vadasery, Nagercoil, Tn, IN) from 1992 to 1999: 6 510(k) clearances. Most are in product codes LZA (Polymer Patient Examination Glove) 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, general hospital panel, where it files most

How often FDA has decided Sri Anusham Rubber Industries Pvt., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sri Anusham Rubber Industries Pvt., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sri Anusham Rubber Industries Pvt., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sri Anusham Rubber Industries Pvt., 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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