510(k) Report

FDA applicant

Ta Chia Rubber Ind. Corp.

Ta Chia, Taichung, TW2 decisions1999–19990 recalls

FDA records 2 decisions for Ta Chia Rubber Ind. Corp. (Ta Chia, Taichung, TW) in 1999: 2 510(k) clearances. All are in product code LZA (Polymer 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 Ta Chia Rubber Ind. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ta Chia Rubber Ind. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ta Chia Rubber Ind. Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ta Chia Rubber Ind. Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • LZAPolymer Patient Examination Glove2decisions

What has FDA decided for it lately?

  • K990577TA Chia Powder Free Non-Sterile Nitrile Patient Examination GlovesTa Chia Rubber Ind. Corp. · 1999
  • K990575TA Chia Powdered Non-Sterile Nitrile Patient Examination GlovesTa Chia Rubber Ind. Corp. · 1999

All 2 as Ta Chia Rubber Ind. Corp. →