PRESERVATION SOLUTIONS, INC.

FDA Device Registration & Listing · ELKHORN, WI, US · Registration 2132588

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
2132588
FEI Number
1000221028
Entity Name
PRESERVATION SOLUTIONS, INC.
City/State/Country
ELKHORN, WI, US
Establishment Address
1099 Proctor Dr, ELKHORN, WI 53121, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PRESERVATION SOLUTIONS, INC. (Owner Number: 9010760)
Owner / Operator Contact Address
1099 PROCTOR DR., P.O.BOX 937, Elkhorn, WI 53121, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K080432
PMA Number
N/A

All Registered Proprietary Names

ClearIt Anti-Fog Solution ClearIt Anti-Fog Cloth Jac-cell Medic Anti-Fog Cloth ClearIt Anti-Fog Kits TAWT - TransAbdominal Wall Traction Device or StarGuard Wittmann Patch MaPerSol Organ Preservation Solution Machine Perfusion Sol'n-Belzer MPS Waters IGL Pulsatile Perfusion Sol.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OCT Anti Fog Solution And Accessories, Endoscopy Gastroenterology, Urology Class 2 876.1500 2007-12-04
KGS Retention Device, Suture General, Plastic Surgery Class 1 878.4930 2012-08-28
FTL Mesh, Surgical, Polymeric General, Plastic Surgery Class 2 878.3300 2012-08-28
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2008-12-31

Official Correspondent

Bobbi Rader

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PRESERVATION SOLUTIONS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K220540 Covidien ProGrip Self-Gripping Polypropylene Mesh 2022-09-22
K013575 Organ Recovery Systems, Inc. KPS-I, THE KIDNEY PERFUSION SOLUTION 2002-01-25

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2132588. Last updated year: 2026. Please use registration number 2132588 when referencing this establishment in official correspondence.
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