About Maxter Gloves USA

Maxter Health: Advancing the vision established by Supermax

Maxter is a proud U.S. subsidiary of Supermax Corporation, a globally recognized leader in medical disposable PPE, exporting to over 165 countries.

Global Reach: Offices and distribution centers in the US, Canada, Brazil, Ireland, UK, Japan, Hong Kong, and Singapore.
Manufacturing Presence: 18 Manufacturing plants globally to include Texas facility; medical face mask facility in Canada
Own Brands: Flagship brands include Aurelia, Supermax, Maxter, and Elevate (exclusive U.S. manufacturing).

Supermax Established: 1987 (38 years experience)

Maxter Health Established: 2021

MHI Valued Proposition: Comprehensive glove portfolio, scalable, dedicated production lines to meet market demand, direct shipping, and warehousing in Houston and Chicago to support consistent, demand-driven supply and reduce risk through multiple shipping locations.

Strategically located in Rosharon, Texas

Approx 60 minutes from Houston’s International airports
45 minutes from the Port of Houston
30 minutes south of the Houston Medical Center

90% of the US can be reached within 2 days of shipping

215 Acre Campus (Expandable)
1.8 Million square feet
Solar Energy -5580 panels
On-site wastewater treatment
1+ Million gallons/day/building

Production Capabilities

Cutting-Edge Manufacturing

Phase 1 Production Overview

~4.8 billion gloves annually upon Phase 1 completion
Four planned phases to reach over 19 billion gloves per year (19 million cases)

Advanced Manufacturing Technology

Highly automated, robotic production lines and packing stations
Artificial Intelligence visual inspection powered by NVIDIA technology, ensuring 99.99% accuracy in defect detection
Dual-High Speed Efficiency Dipping Lines

Strategic Product Focus

disposable nitrile gloves for healthcare, retail, industrial, MRO, automotive, janitorial and food service sectors

Innovation & Continuous Improvement

On-site R&D Center dedicated to advancing product features and optimizing production processes

World-Class Certifications

Certified to ISO 9001, ISO 13485, 21 CFR 820, and MDSAP (Medical Device Single Audit Program)

Engineering Highlights

Innovative Infrastructure

WWTP capacity – treat 1 million gallons / day per manufacturing building
Solar Output Capacity – 4MW (5,580 total panels)
Electric Demand Load – 12MW / manufacturing building
Total Tons of Steel – 5,459 tons
X’ LF of Trench Drains – 8,000LF
Total Deep Foundations/ACP – 1,825 total Auger Cast Piles (ACP) - 1,380 were for the Production Lines
Gas Demand Load – 5billion BTU/day per building
LF of wire – 400,000 LF
Tons of cooling capacity – 1,500TN building + 1,080TN process per manufacturing building

Commitment to Quality

American-Made Excellence

Complies with FDA Medical Device Regulation for Class 1 medical devices (21 CFR 880.6250) and general controls (21 U.S.C. 360c(a)(1)(A)).
Meets ASTM D6319 specifications for Freedom from Holes, Physical Dimensions Test, Physical Requirement Test, and Packaging.
Conforms to ASTM D5511 and D5526 standards for anaerobic biodegradation testing.
Follows ASTM D6978-05 for resistance to chemotherapy drug permeation and Fentanyl resistance in medical gloves.
Adheres to EEC regulations for materials in contact with food (Regulation EEC 1935/2004, EC 10/2011, and EC 2023/2006).
Compliant with FDA 21 CFR 177.2600 for food contact; ASTM D412, D471, and D6284.
Manufactured in compliance with ISO 9001:2015 and ISO 13485:2016 Quality Management Systems. 8/25 completion
NFPA 1999: Standard on Protective Clothing and Equipment for Emergency Medical Operations
AQL- Exceeding industry standard (1.5)