FDA applicant

Elm Tree Medical, Inc.

San Francisco, CA1 decision2017–20170 recalls

FDA records 1 decision for Elm Tree Medical, Inc. (San Francisco, CA) in 2017: 1 510(k) clearance. All are in product code LZA (Polymer 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 Elm Tree Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Elm Tree Medical, Inc. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Elm Tree Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?