Data / Medical devices / Holding Chambers, Direct Patient Interface / United States
FDA-registered makers of Holding Chambers, Direct Patient Interface in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Holding Chambers, Direct Patient Interface (product code NVP). 4 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
- Holding Chambers, Direct Patient Interface
- Product code
- NVP
- Country
- United States
Makers of Holding Chambers, Direct Patient Interface in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Monaghan Medical Corp. | Plattsburgh, NY, United States | Contract manufacturer, Manufacturer | 4 | January 15, 2025 | 0 | 0 | 0 | api.fda.gov |
| Thayer Medical Corportation | Tucson, AZ, United States | Manufacturer | 2 | April 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| Respironics Inc. | Murrysville, PA, United States | Complaint file establishment, Specification developer | 1 | August 9, 2011 | 0 | 0 | 0 | api.fda.gov |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Manufacturer | 1 | June 5, 2013 | 0 | 0 | 0 | api.fda.gov |
| Nolato GW Tucson | Tucson, AZ, 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.