MAXPERT MEDICAL, LLC

FDA Device Registration & Listing · Galloway, OH, US · Registration 3012750295

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
3012750295
FEI Number
3012750295
Entity Name
MAXPERT MEDICAL, LLC
City/State/Country
Galloway, OH, US
Establishment Address
6106 Bausch Rd, Galloway, OH 43119, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Maxpert Medical, LLC (Owner Number: 10052530)
Owner / Operator Contact Address
PO Box 111, Galloway, OH 43119, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MAXPERT MAXCRUSH Crusher Pouch Crushield Pill Crusher Pouch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2021-03-12
KYW Container, Liquid Medication, Graduated General Hospital Class 1 880.6430 2017-06-19

Official Correspondent

Connie Lewis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Maxpert Medical, 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
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012750295. Last updated year: 2026. Please use registration number 3012750295 when referencing this establishment in official correspondence.
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