COMAR LLC

FDA Device Registration & Listing · Woodville, WI, US · Registration 3010423292

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
3010423292
FEI Number
3010423292
Entity Name
COMAR LLC
City/State/Country
Woodville, WI, US
Establishment Address
104 Park Avenue, Woodville, WI 54028, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Comar LLC (Owner Number: 10080243)
Owner / Operator Contact Address
220 Laurel Rd., Ste. 201, Voorhees, NJ 08043, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

IntelliSep Cartridge

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QUT Deformability Cytometry For Sepsis Risk Assessment Microbiology Class 2 866.3215 2026-03-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
2220100 COMAR, LLC Buena, NJ, US
3019682545 COMAR, LLC East Vineland, NJ, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010423292. Last updated year: 2026. Please use registration number 3010423292 when referencing this establishment in official correspondence.
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