FDA applicant

Full Golden Biotech Corporation

Taichung, TW2 decisions2025–20250 recalls

FDA records 2 decisions for Full Golden Biotech Corporation (Taichung, TW) in 2025: 2 510(k) clearances. All are in product code LYC (Bone Grafting Material, Synthetic). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Full Golden Biotech Co., Ltd.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Full Golden Biotech Corporation’s devices, and how often a recall has named them.

FDA decisions per year

2in 2025

2025high 2 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2025.

FIG. 1 — Full Golden Biotech Corporation by year, 2025–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Full Golden Biotech Corporation’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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Other applicant names beginning “Full”

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

Full Synergy Medical Products, Inc. 6 Full Spectrum, Inc. 3 Full See Glasses Ind. Co., Ltd. 1 Full Power Aed 1

Full Golden Biotech Corporation

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Full”