510(k) Report

FDA applicant

Young OU Brush Co.

Kyong Buk, KR1 decision1997–19970 recalls

FDA records 1 decision for Young OU Brush Co. (Kyong Buk, KR) in 1997: 1 510(k) clearance. All are in product code HHT (Spatula, Cervical, Cytological). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Young OU Brush Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Young OU Brush Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Young OU Brush Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Young”

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