FDA applicant

The Orient Connection

Cincinnati, OH1 decision1989–19890 recalls

FDA records 1 decision for The Orient Connection (Cincinnati, OH) 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 The Orient Connection’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Orient Connection since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Orient Connection by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “The”

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

Orient Commercial Co., Ltd. 1 Orient Intl. Trading, Inc. 1 Orient Gene Biotech 1

The Orient Connection

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”