510(k) Report

FDA applicant

Thai Fuji Latex Co., Ltd.

San Francisco, CA1 decision1990–19900 recalls

FDA records 1 decision for Thai Fuji Latex Co., Ltd. (San Francisco, CA) in 1990: 1 510(k) clearance. All are in product code FGO (Dislodger, Stone, Flexible). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Thai Fuji Latex Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thai Fuji Latex Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Thai Fuji Latex Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Thai Fuji Latex Co., Ltd.’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

Other applicant names beginning “Thai”

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