VITALCOR, INC.

FDA Device Registration & Listing · WESTMONT, IL, US · Registration 1450019

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
1450019
FEI Number
1450019
Entity Name
VITALCOR, INC.
City/State/Country
WESTMONT, IL, US
Establishment Address
100 EAST CHESTNUT AVE., WESTMONT, IL 60559, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Vitalcor, Inc. (Owner Number: 1450019)
Owner / Operator Contact Address
100 Chestnut Ave, --, Westmont, IL 60559, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Britetrac Retractor Applied Fiberoptics a division of Vitalcor, Inc. Vitalcor, Inc. Vitalcor, Inc. Gemini Plus Applied Fiberoptics a division of Vitalcor, Inc. Vitalcor, Inc. Vitalcor Featherweight Vasc, Clamp Dingo Vascular Clamp Applied Fiberoptics

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FDG Retractor, Fiberoptic Gastroenterology, Urology Class 1 876.4530 2016-09-02
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2016-09-02
FHQ Holder, Needle, Gastroenterologic Gastroenterology, Urology Class 1 876.4730 2016-09-02
FCT Headlight, Fiberoptic Focusing Ophthalmic Class 2 886.4335 2016-09-02
GEN Forceps, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2016-09-02
DXC Clamp, Vascular Cardiovascular Class 2 870.4450 2007-12-28

Official Correspondent

R Gregory Huck

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vitalcor, Inc.
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
K851170 The Huxley Instrument Corp. DISSECTING TWEEZER #283-72PCS. SS 410 1985-04-25
K821248 Conphar, Inc. ROCHESTER PEAN FORCEPS 1982-05-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1450019. Last updated year: 2026. Please use registration number 1450019 when referencing this establishment in official correspondence.
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