Data / Medical devices / Anti Fog Solution And Accessories, Endoscopy / United States
FDA-registered makers of Anti Fog Solution And Accessories, Endoscopy in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Anti Fog Solution And Accessories, Endoscopy (product code OCT). 8 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Anti Fog Solution And Accessories, Endoscopy
- Product code
- OCT
- Country
- United States
Makers of Anti Fog Solution And Accessories, Endoscopy in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 2 | January 22, 2019 | 0 | 0 | 0 | api.fda.gov |
| Key Surgical, LLC | Eden Prairie, MN, United States | Complaint file establishment, Specification developer | 2 | March 3, 2000 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Complaint file establishment, Specification developer | 2 | February 4, 2016 | 0 | 0 | 0 | api.fda.gov |
| Covidien | North Haven, CT, United States | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 1 | March 25, 1994 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Ponce, PR, United States | Contract manufacturer, Manufacturer | 1 | March 25, 1994 | 0 | 0 | 0 | api.fda.gov |
| Deroyal Industries, Inc. | Powell, TN, United States | Complaint file establishment, Specification developer | 1 | August 11, 1998 | 0 | 0 | 0 | api.fda.gov |
| Preservation Solutions, Inc. | Elkhorn, WI, United States | Contract manufacturer, Manufacturer | 1 | October 9, 2002 | 0 | 0 | 0 | api.fda.gov |
| Xodus Medical, Inc. | New Kensington, PA, United States | Manufacturer | 1 | January 9, 2007 | 0 | 0 | 0 | api.fda.gov |
| ConMed Corporation | Greenwood Village, CO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtronic Distribution Center | Memphis, TN, United States | Manufacturer | 0 | 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.