MAR-MED Inc.

FDA Device Registration & Listing · Grand Rapids, MI, US · Registration 1832653

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
1832653
FEI Number
1832653
Entity Name
MAR-MED Inc.
City/State/Country
Grand Rapids, MI, US
Establishment Address
333 Fuller Ave NE, Grand Rapids, MI 49503, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Mar-Med Inc, (Owner Number: 1832653)
Owner / Operator Contact Address
333 Fuller NE, Grand Rapids, MI 49503, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K853472
PMA Number
N/A

All Registered Proprietary Names

Supershield SplashShield Klenzalac ZeroWet Derma-Stent Balloon Extractor Tourni-Cot

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYZ Syringe, Irrigating (Non Dental) General Hospital Class 1 880.6960 2025-12-23
GBX Catheter, Irrigation General, Plastic Surgery Class 1 878.4200 2016-10-12
KBE Snare, Nasal Ear, Nose, Throat Class 1 874.4420 2016-10-30
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2009-12-28

Official Correspondent

Joel Marogil

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mar-Med Inc,
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1832653. Last updated year: 2026. Please use registration number 1832653 when referencing this establishment in official correspondence.
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