FDA applicant

Glen Nevis Co.

South San Francisco, CA1 decision1989–19890 recalls

FDA records 1 decision for Glen Nevis Co. (South San Francisco, CA) 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 Glen Nevis Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Glen Nevis Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Glen Nevis Co.’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 “Glen”

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

Glen Whitten, Dds 4

Glen Nevis Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Glen”