Penner Patient Care, INC

FDA Device Registration & Listing · Aurora, NE, US · Registration 1922538

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
1922538
FEI Number
1922538
Entity Name
Penner Patient Care, INC
City/State/Country
Aurora, NE, US
Establishment Address
101 Grant St, Aurora, NE 68818, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Penner Patient Care, INC (Owner Number: 9041224)
Owner / Operator Contact Address
101 GRANT ST., Aurora, NE 68818, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K040772
PMA Number
N/A

All Registered Proprietary Names

PACIFIC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILJ Bath, Hydro-Massage Physical Medicine Class 2 890.5100 2007-11-26

Official Correspondent

Dean Amundson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Penner Patient Care, INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1922538. Last updated year: 2026. Please use registration number 1922538 when referencing this establishment in official correspondence.
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