FDA applicant

Glyde USA, Inc.

Redmond, WA1 decision1998–19980 recalls

FDA records 1 decision for Glyde USA, Inc. (Redmond, WA) in 1998: 1 510(k) clearance. All are in product code MSC (Barrier, Std, Oral Sex). 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 Glyde USA, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Glyde USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Glyde USA, Inc.’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

Glyde USA, Inc.

Which product codes does it file in?

What has FDA decided for it lately?