ILC Dover

FDA Device Registration & Listing · Lillington, NC, US · Registration 3038515260

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
3038515260
FEI Number
3038515260
Entity Name
ILC Dover
City/State/Country
Lillington, NC, US
Establishment Address
900 Edwards Brothers Dr, Lillington, NC 27546, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ILC Dover (Owner Number: 10055941)
Owner / Operator Contact Address
1 Moonwalker Road, Frederica, DE 19946, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EasiSlush

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2023-12-19

Official Correspondent

Sommer Altvater

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ILC Dover
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
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 3038515260. Last updated year: 2026. Please use registration number 3038515260 when referencing this establishment in official correspondence.
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