FDA applicant

Entellus Medical, Inc. (Aka Stryker Ent)

Plymouth, MN1 decision2019–20190 recalls

FDA records 1 decision for Entellus Medical, Inc. (Aka Stryker Ent) (Plymouth, MN) in 2019: 1 510(k) clearance. All are in product code NHB (Polymer, Ear, Nose And Throat, Synthetic…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, ear, nose and throat panel, where it files most

How often FDA has decided Entellus Medical, Inc. (Aka Stryker Ent)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Entellus Medical, Inc. (Aka Stryker Ent) by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Entellus Medical, Inc. (Aka Stryker Ent)’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

Other applicant names beginning “Entellus”

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

Entellus Medical, Inc. 27

Entellus Medical, Inc. (Aka Stryker Ent)

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Entellus”