Caresfield LLC

FDA Device Registration & Listing · Lakeville, MN, US · Registration 3008872935

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
3008872935
FEI Number
3008872935
Entity Name
Caresfield LLC
City/State/Country
Lakeville, MN, US
Establishment Address
8095 215th St W, Lakeville, MN 55044, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Caresfield LLC (Owner Number: 10035346)
Owner / Operator Contact Address
8095 215th Street West, Lakeville, MN 55044, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tourniquet Absorbent

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2011-02-22
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2015-04-30

Official Correspondent

Steve Griffith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Caresfield LLC
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 3008872935. Last updated year: 2026. Please use registration number 3008872935 when referencing this establishment in official correspondence.
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