510(k) Report

FDA applicant

Inter-Asia Co., Inc.

Woodinville, WA1 decision1989–19890 recalls

FDA records 1 decision for Inter-Asia Co., Inc. (Woodinville, WA) in 1989: 1 510(k) clearance. All are in product code 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 Inter-Asia Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inter-Asia Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inter-Asia Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Inter-Asia Co., Inc.’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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Which product codes does it file in?

  • LYYLatex Patient Examination Glove1decision

What has FDA decided for it lately?

  • K893180Sensifit (R) Latex Examination GlovesInter-Asia Co., Inc. · 1989

The one decision as Inter-Asia Co., Inc. →

Other applicant names beginning “Inter-Asia”

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

Inter-Med, Inc. 12Inter-Med/Vista Dental Products 6Inter Medical Medizintechnik GmbH 3Inter Med Industries, Inc. 3Inter Science Institute 3Inter-Os Technologies 2Inter Continental Health Care 2Inter-Pal GmbH 1Inter-Med / Vista Dental 1Inter-Continental Industries Sdn Bhd 1