Data / Medical devices / Surgeon'S Gloves / United States
FDA-registered makers of Surgeon'S Gloves in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Surgeon'S Gloves (product code KGO). 10 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Surgeon'S Gloves
- Product code
- KGO
- Country
- United States
Makers of Surgeon'S Gloves in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ansell Healthcare Products LLC | Reno, NV, United States | Manufacturer, Specification developer | 23 | October 20, 2023 | 0 | 2 | 0 | api.fda.gov |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 17 | September 26, 2021 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Complaint file establishment, Specification developer | 10 | August 2, 2021 | 0 | 2 | 1 | api.fda.gov |
| Prestige Ameritech | North Richland Hills, TX, United States | Complaint file establishment, Specification developer | 6 | March 9, 2016 | 0 | 0 | 0 | api.fda.gov |
| CT Intl. | San Luis Obispo, CA, United States | Specification developer | 3 | August 5, 1999 | 0 | 0 | 0 | api.fda.gov |
| Avid Medical, Inc. A Medical Action Ind. Company 305 | Toano, VA, United States | Manufacturer, Repackager or relabeler | 2 | July 7, 2011 | 0 | 0 | 0 | api.fda.gov |
| Medical Action Industries, Inc. 306 | Arden, NC, United States | Manufacturer, Repackager or relabeler | 2 | July 7, 2011 | 0 | 0 | 0 | api.fda.gov |
| Infab, LLC. | Camarillo, CA, United States | Manufacturer | 1 | March 21, 2003 | 0 | 0 | 0 | api.fda.gov |
| LDI Solutions, LLC | Rochester, NH, United States | Specification developer | 1 | June 27, 2019 | 0 | 0 | 0 | api.fda.gov |
| SW Technologies Inc. | Union City, CA, United States | Manufacturer | 1 | March 29, 2012 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.