510(k) Report

FDA applicant

Everrise Glove Products Co., Ltd.

Tainan Hsien, TW2 decisions1997–19970 recalls

FDA records 2 decisions for Everrise Glove Products Co., Ltd. (Tainan Hsien, TW) in 1997: 2 510(k) clearances. All are in product code LYZ (Vinyl 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 Everrise Glove Products Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Everrise Glove Products Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • LYZVinyl Patient Examination Glove2decisions

What has FDA decided for it lately?

  • K973998Vinyl Patient Examination Gloves Powder-FreeEverrise Glove Products Co., Ltd. · 1997
  • K973902Vinyl Patient Examination Gloves PowderedEverrise Glove Products Co., Ltd. · 1997

All 2 as Everrise Glove Products Co., Ltd. →