3-Ply Protective Masks (boxes of 50)



50 pcs per box

Min order 4 boxes (200 pcs)

Companies that export products from the United States are often asked by foreign customers or officials to provide a "certificate" for products regulated by the Food and Drug Administration (FDA). A FDA certificate is a document prepared by the FDA containing information on the regulatory or commercial status of a product.
There are numerous unqualified FDA certifications provided by different suppliers. But, you can check ours by simply clicking here. On the official FDA website, our registration number is 3008111543.
Also, 3-ply and KN95 masks both require a different set of FDA product code registration. Our factory has both the codes registered.



Compared to KN95 masks, 3-Ply protective masks need to be tested on another filtration level. The purpose of the test is to verify the durability of the masks against bacteria and other harmful pathogens. The term is called bacteria filtration efficiency and particle filtration efficiency.
The test report provided is conducted by GTT which is a testing organisation which is a reputed member of CNAS testing (China National Accreditation Service for Conformity Assessment).

As shown of the test reports, our 3-Ply protective masks are tested 99%+ effective in terms of BFE and PFE.


In China, all businesses are required to comply with standard rules implemented by the Chinese government. Every legitimate business in China will have a registered business license. This license is essential to prove the legitimacy of the business and to provide a deeper understanding on the scopes of the business.

The factory we work with is qualified to manufacture PPE (personal protective equipment) such as masks and other medical products.

The license is vital for any export out of China. Any factory that fails to provide this license proving the scope of their business will not be able to pass the customs clearance ( as of the new rule implemented on April 1st ).


A quality management system (QMS) is a collection of business processes focused on consistently meeting customer requirements and enhancing their satisfaction.

The factory we work with complies with the following:

1. GMP

Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimise the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. 

Our factory's GMP certificate has been assessed by Intertek, which is renowned for its product testing, inspection and reassurance services. The GMP certificate affirms that our has good reliable manufacturing practices in the fields of medical products.

2. SA8000

SA 8000 is an international certification standard that encourages organisations to develop, maintain and apply socially acceptable practices in the workplace. 

Our Factory thrives for good manufacturing practices for our customers and also our workers.




Transit time - 8 to 10 working days

Tracking number provided

Custom clearance ( Handled by us ) 


Box dimension : 19x10x10cm
N.W. : 155g
G.W. : 203g
Carton dimension : 51.5x39x42cm
N.W. : 5.6kg
G.W. : 9.3kg