FDA applicant

Medline Renewal

Redmond, OR1 decision2014–20140 recalls

FDA records 1 decision for Medline Renewal (Redmond, OR) in 2014: 1 510(k) clearance. All are in product code NLY (Microdebrider, Ent, High Speed, Single Use…). 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 Medline Renewal’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Medline Renewal by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Medline”

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

Medline Industries, Inc. 269 Medline 11 Medline Industires, Inc. 6 Medline Products Co., Ltd. 1

Medline Renewal

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Medline”