SIM Med, LLC

FDA Device Registration & Listing · Sussex, WI, US · Registration 3008972967

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
3008972967
FEI Number
3008972967
Entity Name
SIM Med, LLC
City/State/Country
Sussex, WI, US
Establishment Address
N65W24770 Main St., Sussex, WI 53089, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SIM-MED, LLC (Owner Number: 10081377)
Owner / Operator Contact Address
N65W24770 Main St., Sussex, WI 53089, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Q-Collar

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QNX External Compression Device For Internal Jugular Vein Compression Neurology Class 2 890.3050 2021-04-08

Official Correspondent

Bau Serratos

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SIM-MED, 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 3008972967. Last updated year: 2026. Please use registration number 3008972967 when referencing this establishment in official correspondence.
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