Data / Medical devices / Anaerobic Box Glove

Anaerobic Box Glove (JTM): 17 FDA-registered makers in 4 countries

Name: FDA-registered makers of Anaerobic Box Glove
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

17 establishments in 4 countries are registered with the FDA to make Anaerobic Box Glove (product code JTM, Class 1, 21 CFR 866.2120). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on April 2, 1980, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code: JTM
Device class: 1
Regulation: 866.2120
Medical specialty: Microbiology

Makers by country

Country	Makers
China	8
United States	6
India	2
Vietnam	1

Makers of Anaerobic Box Glove

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Maker	Location	Role	Source
Anaerobe Systems	Morgan Hill, CA, United States	Complaint file establishment, Manufacturer	api.fda.gov
Bestreat Safety & First Aid Solution Co., Ltd	Wuhan Hubei, China	Manufacturer	api.fda.gov
Comatrix Technology Vietnam Company Limited	Ho Chi Minh City, Vietnam	Contract manufacturer, Manufacturer	api.fda.gov
Gauke (hubei) Healthcare Co., Ltd	Huanggang City Hubei, China	Contract manufacturer, Manufacturer, Repackager or relabeler	api.fda.gov
Greens Surgicals Private Limited	Vadodara Gujarat, India	Manufacturer	api.fda.gov
Hager Worldwide, Inc.	Hickory, NC, United States	Complaint file establishment, Specification developer	api.fda.gov
Jinhua Jingdi Medical Supplies Co.,ltd	Jinhua Zhejiang, China	Exporter to the US, Manufacturer	api.fda.gov
K&R Technologies Dba Microbiology International	Frederick, MD, United States	Specification developer	api.fda.gov
Ningbo Tianbo First Aid Product Co., Ltd.	Ningbo Zhejiang, China	Manufacturer	api.fda.gov
Sheldon MFG., Inc.	Cornelius, OR, United States	Manufacturer	api.fda.gov
STS Corporation	Duluth, GA, United States	Complaint file establishment, Repackager or relabeler, Specification developer	api.fda.gov
Shanghai Joy Crown Industry Co., Ltd	Pu Dong New Area Shanghai, China	Contract manufacturer	api.fda.gov
Tegamen Safety Products Pvt. Ltd.	Alwar Rajasthan, India	Manufacturer	api.fda.gov
Thermo Fisher Scientific (asheville) LLC	Marietta, OH, United States	Manufacturer	api.fda.gov
Yangzhou Feiyali Sporting Goods Co.ltd	Yangzhou Jiangsu, China	Contract manufacturer, Manufacturer	api.fda.gov
Zhejiang Banghaoning Medical Supplies Co., Ltd	YiWu Zhejiang, China	Manufacturer	api.fda.gov
Zhejiang Excellent United Medical Technology Co.,ltd	Jinhua Zhejiang, China	Exporter to the US, Manufacturer	api.fda.gov

Updated April 2, 1980. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.