CHAMBERLAIN TECHNOLOGIES, LLC

FDA Device Registration & Listing · Deer Park, IL, US · Registration 3015860534

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
3015860534
FEI Number
3015860534
Entity Name
CHAMBERLAIN TECHNOLOGIES, LLC
City/State/Country
Deer Park, IL, US
Establishment Address
21805 W Field Parkway, Suite 160, Deer Park, IL 60010, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Chamberlain Technologies, LLC (Owner Number: 10061294)
Owner / Operator Contact Address
21805 W Field Parkway, Suite 160, Deer Park, IL 60010, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K061445
PMA Number
N/A

All Registered Proprietary Names

SurgiMesh WN

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FTL Mesh, Surgical, Polymeric General, Plastic Surgery Class 2 878.3300 2019-10-04

Official Correspondent

John Huelskamp

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Chamberlain Technologies, LLC
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015860534. Last updated year: 2026. Please use registration number 3015860534 when referencing this establishment in official correspondence.
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