Peytant Solutions

FDA Device Registration & Listing · Plymouth, MN, US · Registration 3013847376

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013847376
FEI Number
3013847376
Entity Name
Peytant Solutions
City/State/Country
Plymouth, MN, US
Establishment Address
3650 Annapolis Lane North 180, Plymouth, MN 55447, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Peytant Solutions (Owner Number: 10094039)
Owner / Operator Contact Address
3650 Annapolis Lane North 180, Plymouth, MN 55447, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
DEN230087
PMA Number
N/A

All Registered Proprietary Names

AMStent Tracheobronchial Covered Stent System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SDB Tracheal Prosthesis With Cover Material Derived From Human Sources Anesthesiology Class 2 868.3721 2025-12-08

Official Correspondent

Lou Ellis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Peytant Solutions
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013847376. Last updated year: 2026. Please use registration number 3013847376 when referencing this establishment in official correspondence.
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