myONE N99/53H

2 catalogue numbers from MYONE-N99/53H-12, listed by Global Protection Corp., United States, under Condom. 9 manufacturers in China are registered for this product code.

Registry build 21.09.26
9manufacturers in China registered for this device type
2catalogue numbers in this listing
4510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (2), Guangdong (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HIS
Manufacturer City Province Registered as Device types
Suzhou Armocon Technology Co., Ltd. Jiangsu Jiangsu Contract manufacturer 5
Dalian Latex Co Ltd Dalian Liaoning Contract manufacturer 1
Rfx+care Manufacturing Co., Ltd. Shaoxing Zhejiang Repacker / relabeller 21
Suzhou Colour-way New Material Co., Ltd. Suzhou Jiangsu Manufacturer 5
Shanghai Jinxiang Latex Products Co., Ltd. Shanghai Shanghai Contract manufacturer 3
Shanghai Personage Hygiene Products Co., Ltd. Shanghai Shanghai Manufacturer 1
Guangzhou Double One Latex Products Co., Ltd. Guangzhou Guangdong Contract manufacturer 1
Qingdao London Durex Co., Ltd. Qingdao Shandong Manufacturer 1
Shaoguan Regenex Pharmaceutical Co., Ltd. Shaoguan Guangdong Manufacturer 1

Record

Regulatory record for myONE N99/53H
Listed by Global Protection Corp., United States
FDA product code HIS
Device type Condom
Device class Class 2
Regulation 21 CFR 884.5300
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2023-03-28
Record revised 2023-10-31 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Over the counter Yes
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for myONE N99/53H
Catalogue number Size Per pack Status
MYONE-N99/53H-12 12 In distribution
MYONE-N99/53H-36 36 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Lifestyles Suretex Limited – Branch 158
Custom Condoms Global Protection Corp. 94
My One Global Protection Corp. 51
ONE Global Protection Corp. 45
Keypers Global Protection Corp. 38
Handy Solutions Navajo Manufacturing Company 35
Royal M3 Global Enterprises, LLC 26
b condoms B Holding Group LLC 22
ONE Lunamax LLC 20
Kimono Mayer Laboratories 20
Trustex lubricated Condoms Global Protection Corp. 18
Primeros Richter Rubber Technology SDN. BHD. 18

Showing 12 of 688. All products under Condom

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K203536 2021-09-03
K193578 2020-08-20
K024324 2003-03-25
K960552 1997-11-20

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2007-09-11 Not classified Process control Condoms fail the water leak test and package integrity 127,00 condoms 2008-03-18

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer