HEATHROW SCIENTIFIC, LLC

FDA Device Registration & Listing · Vernon Hills, IL, US · Registration 3003510542

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
3003510542
FEI Number
3003510542
Entity Name
HEATHROW SCIENTIFIC, LLC
City/State/Country
Vernon Hills, IL, US
Establishment Address
440 N Fairway Dr, Vernon Hills, IL 60061, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Heathrow Scientific, LLC (Owner Number: 10081165)
Owner / Operator Contact Address
440 N. Fairway Drive, Vernon Hills, IL 60061, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Centrifuge (Micro) Curette, surgical, general use

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2022-06-23
FZS Curette, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2025-02-18

Official Correspondent

Nicole Smokowicz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2012 X Spine Systems Inc 1
Axle Interspinous Fusion System Torque Driver Handle, Model #: X060-0323, Lot # 525941, S/Ns 001-017, Lot # 525942, S/Ns 001-050, Mfr. By: Bradshaw Medical Inc., Kenosha, WI 53144 The Axle Torque Driver Handle is used to lock the set screw into the locking plate.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003510542. Last updated year: 2026. Please use registration number 3003510542 when referencing this establishment in official correspondence.
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