FDA applicant

Brightway Gloves Pvt., Ltd.

Tamil Nadu, IN4 decisions2002–20020 recalls

FDA records 4 decisions for Brightway Gloves Pvt., Ltd. (Tamil Nadu, IN) in 2002: 4 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Brightway Gloves Pvt., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Brightway Gloves 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 “Brightway”

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

Brightway Holdings Sdn. Bhd. 24

Brightway Gloves Pvt., Ltd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Brightway”