Data / Medical devices / Accessories, Cleaning, For Endoscope / United States
FDA-registered makers of Accessories, Cleaning, For Endoscope in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Accessories, Cleaning, For Endoscope (product code FEB). 12 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.
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- Device
- Accessories, Cleaning, For Endoscope
- Product code
- FEB
- Country
- United States
Makers of Accessories, Cleaning, For Endoscope in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medivators Inc | Minneapolis, MN, United States | Complaint file establishment, Manufacturer, Manufacturer for export, Specification developer | 8 | October 2, 2026 | 0 | 1 | 0 | api.fda.gov |
| Advanced Sterilization Products | Irvine, CA, United States | Complaint file establishment, Specification developer | 4 | April 23, 2019 | 0 | 6 | 0 | api.fda.gov |
| STERIS Corporation | Mentor, OH, United States | Manufacturer, Repackager or relabeler | 3 | October 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Wassenburg Medical, Inc. | Ivyland, PA, United States | Manufacturer | 3 | December 19, 2024 | 0 | 1 | 0 | api.fda.gov |
| Medivators Inc | Conroe, TX, United States | Manufacturer | 2 | January 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| Steris Corporation | Mentor, OH, United States | Specification developer | 2 | December 2, 2024 | 0 | 4 | 0 | api.fda.gov |
| STERIS Corporation | Mentor, OH, United States | Manufacturer | 2 | December 2, 2024 | 0 | 0 | 0 | api.fda.gov |
| Covidien | North Haven, CT, United States | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 1 | September 20, 1994 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Ponce, PR, United States | Contract manufacturer, Manufacturer | 1 | September 20, 1994 | 0 | 0 | 0 | api.fda.gov |
| Hobbs Medical, Inc. | Stafford Springs, CT, United States | Contract manufacturer, Manufacturer | 1 | October 28, 1993 | 0 | 0 | 0 | api.fda.gov |
| Steris Corporation | Saint Louis, MO, United States | Manufacturer | 1 | October 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| TeleMed Systems | Northborough, MA, United States | Specification developer | 1 | June 11, 1990 | 0 | 0 | 0 | api.fda.gov |
| Allwin Medical Devices, Inc. | Anaheim, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Inc. | Auburn Hills, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.