Data / Medical devices / Anoscope And Accessories / United States
FDA-registered makers of Anoscope And Accessories in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Anoscope And Accessories (product code FER). 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
- Anoscope And Accessories
- Product code
- FER
- Country
- United States
Makers of Anoscope And Accessories in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Applied Medical Resources Corp. | Rsm, CA, United States | Complaint file establishment, Manufacturer | 2 | July 20, 2017 | 0 | 1 | 0 | api.fda.gov |
| Applied Medical Distribution Center | Irvine, CA, United States | Manufacturer | 2 | July 20, 2017 | 0 | 0 | 0 | api.fda.gov |
| Coopersurgical, Inc. | Trumbull, CT, United States | Complaint file establishment, Manufacturer, Specification developer | 2 | July 27, 2012 | 0 | 0 | 0 | api.fda.gov |
| Welch Allyn, Inc. | Skaneateles Falls, NY, United States | Manufacturer, Specification developer | 2 | February 19, 1981 | 0 | 0 | 0 | api.fda.gov |
| Gastro Concepts | Albuquerque, NM, United States | Manufacturer | 1 | December 13, 2024 | 0 | 0 | 0 | api.fda.gov |
| OBP Medical Corporation | Lawrence, MA, United States | Specification developer | 1 | July 27, 2012 | 0 | 0 | 0 | api.fda.gov |
| CARCLO TECHNICAL PLASTICS - Greensburg | Greensburg, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carclo Technical Plastics - Latrobe | Latrobe, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | North Haven, CT, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtronic Distribution Center | Memphis, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STERIS Corporation | Saint Louis, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weco Manufacturing Group-Henrietta | Rochester, NY, United States | Manufacturer, Repackager or relabeler | 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.