PROGIA MEDICAL INC.

FDA Device Registration & Listing · Plymouth, MN, US · Registration 3032328006

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
3032328006
FEI Number
3032328006
Entity Name
PROGIA MEDICAL INC.
City/State/Country
Plymouth, MN, US
Establishment Address
14495 23rd Avenue North, Plymouth, MN 55447, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Progia Medical Inc. (Owner Number: 10091373)
Owner / Operator Contact Address
14495 23rd Avenue North, Plymouth, MN 55447, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Swallow Therapy System (STS) Progia Medical Insta™

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKE Transducer, Miniature Pressure Physical Medicine Class 1 890.1615 2024-09-09

Official Correspondent

Ross Dunbar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Progia Medical Inc.
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 3032328006. Last updated year: 2026. Please use registration number 3032328006 when referencing this establishment in official correspondence.
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