510(k) Report

FDA applicant

Peytant Solutions, Inc.

Plymouth, MN1 decision2024–20240 recalls

FDA records 1 decision for Peytant Solutions, Inc. (Plymouth, MN) in 2024: 1 De Novo grant. All are in product code SDB (Tracheal Prosthesis With Cover Material…). 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, anesthesiology panel, where it files most

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

FDA decisions per year

1in 2024

2024: 1
2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Peytant Solutions, Inc. by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Peytant Solutions, Inc.’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