FDA applicant

Full See Glasses Ind. Co., Ltd.

Taipe, Taiwan, TW1 decision1985–19850 recalls

FDA records 1 decision for Full See Glasses Ind. Co., Ltd. (Taipe, Taiwan, TW) in 1985: 1 510(k) clearance. All are in product code HQG (Lens, Spectacle, Non-Custom (Prescription)). 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, ophthalmic panel, where it files most

How often FDA has decided Full See Glasses Ind. Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Full See Glasses Ind. Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Full See Glasses Ind. Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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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 Golden Biotech Corporation 2 Full Power Aed 1

Full See Glasses Ind. Co., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Full”