Data / Medical devices / Pump, Air, Non-Manual, For Endoscope / United States
FDA-registered makers of Pump, Air, Non-Manual, For Endoscope in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Pump, Air, Non-Manual, For Endoscope (product code FEQ). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Pump, Air, Non-Manual, For Endoscope
- Product code
- FEQ
- Country
- United States
Makers of Pump, Air, Non-Manual, For Endoscope in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| United States Endoscopy Group, Inc. | Mentor, OH, United States | Complaint file establishment, Manufacturer | 4 | August 1, 2019 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Marlborough, MA, United States | Complaint file establishment, Specification developer | 2 | June 27, 2016 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Johns Creek, GA, United States | Manufacturer | 2 | June 27, 2016 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Coventry, RI, United States | Manufacturer | 2 | June 27, 2016 | 0 | 0 | 0 | api.fda.gov |
| Erbe Medical, LLC | Tempe, AZ, United States | Manufacturer, Specification developer | 2 | August 31, 2016 | 0 | 1 | 0 | api.fda.gov |
| Medivators Inc | Conroe, TX, United States | Manufacturer, Specification developer | 2 | March 11, 2022 | 0 | 0 | 0 | api.fda.gov |
| Biotex, Inc. | Houston, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diversatek Healthcare Inc | Milwaukee, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medron, LLC | Salt Lake City, UT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MFG One, LLC | Chantilly, VA, United States | Contract 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.