510(k) Report

FDA applicant

Emanate Biomedical

New York, NY1 decision2026–20260 recalls

FDA records 1 decision for Emanate Biomedical (New York, NY) in 2026: 1 510(k) clearance. All are in product code OLR (Oral Wound Dressing). 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

How often FDA has decided Emanate Biomedical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026 (partial year): 1
2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

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

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Which product codes does it file in?

  • OLROral Wound Dressing1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K251908Emanate TrayEmanate Biomedical · 2026

The one decision as Emanate Biomedical →