510(k) Report

FDA applicant

Kaohsiung Brothers Products Corp.

Kaohsiung, TW4 decisions1989–20030 recalls

FDA records 4 decisions for Kaohsiung Brothers Products Corp. (Kaohsiung, TW) from 1989 to 2003: 4 510(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 Kaohsiung Brothers Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kaohsiung Brothers Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kaohsiung Brothers Products Corp. 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 Glove4decisions

What has FDA decided for it lately?

  • K030200Powdered Synthetic Vinyl Patient Examination Gloves, WhiteKaohsiung Brothers Products Corp. · 2003
  • K003197Vinyl, Powder-Free, Patient Examination Gloves, YellowKaohsiung Brothers Products Corp. · 2000
  • K000058Brothers Powder-Free Vinyl Examination GlovesKaohsiung Brothers Products Corp. · 2000
  • K891336Patient Examination Gloves (Vinyl)Kaohsiung Brothers Products Corp. · 1989

All 4 as Kaohsiung Brothers Products Corp. →