510(k) Report

FDA applicant

Altamira Therapeutics, Inc.

Dover, DE1 decision2022–20220 recalls

FDA records 1 decision for Altamira Therapeutics, Inc. (Dover, DE) in 2022: 1 510(k) clearance. All are in product code NUP (Cream, Nasal, Topical, Mechanical Allergen…). 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, general hospital panel, where it files most

How often FDA has decided Altamira Therapeutics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Altamira Therapeutics, Inc. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NUPCream, Nasal, Topical, Mechanical Allergen Particle Barrier1decision

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?

  • K213114BentrioTM Allergy BlockerAltamira Therapeutics, Inc. · 2022

The one decision as Altamira Therapeutics, Inc. →