Excel Medical Products, Inc.

FDA Device Registration & Listing · Wixom, MI, US · Registration 3004198398

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
3004198398
FEI Number
3004198398
Entity Name
Excel Medical Products, Inc.
City/State/Country
Wixom, MI, US
Establishment Address
28011 Grand Oaks Ct, Wixom, MI 48393, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Excel Medical Products, Inc. (Owner Number: 9056777)
Owner / Operator Contact Address
28011 Grand Oaks Court, --, Wixom, MI 48393, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Excel-4.5 Hemostasis Y-Connector; Excel-6 Hemostasis Y-Connector; Excel-7 Hemostasis Y-Connector; Excel-9 Hemostasis Y-Connector Anatotemp

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2021-12-01
DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass Cardiovascular Class 2 870.4290 2018-12-19
QEW Peripheral Mechanical Thrombectomy With Aspiration Cardiovascular Class 2 870.5150 2026-02-03
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2017-12-21

Official Correspondent

Adam Cole

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Excel Medical Products, 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
K915301 Advance Medical Designs, Inc. ADVANCE STOPCOCK/HIGH PRESSURE STOPCOCK 1992-12-11
K241362 Surmodics,Inc. Pounce XL Thrombectomy System (PTS-1011-7F135) 2024-09-11
K220887 Inari Medical Mini-ClotTriever Thrombectomy System 2022-08-04
K250421 Inari Medical, Inc. InThrill™ Thrombectomy System 2025-05-12
K192036 Inari Medical ClotTriever Thrombectomy System 2019-08-29

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0007-2018 Implant Direct Sybron Manufacturing, LLC 2
Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004198398. Last updated year: 2026. Please use registration number 3004198398 when referencing this establishment in official correspondence.
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