Data / Medical devices / Device, Positive Pressure Breathing, Intermittent / United States
FDA-registered makers of Device, Positive Pressure Breathing, Intermittent in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Device, Positive Pressure Breathing, Intermittent (product code NHJ). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Device, Positive Pressure Breathing, Intermittent
- Product code
- NHJ
- Country
- United States
Makers of Device, Positive Pressure Breathing, Intermittent in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hill-Rom Manufacturing, Inc. | Saint Paul, MN, United States | Manufacturer, Repackager or relabeler | 6 | May 26, 2020 | 0 | 0 | 0 | api.fda.gov |
| Abmrc LLC | Eagan, MN, United States | Complaint file establishment, Manufacturer, Specification developer | 4 | August 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Vortran Medical Technology 1, Inc. | Sacramento, CA, United States | Manufacturer | 2 | February 23, 2001 | 0 | 0 | 0 | api.fda.gov |
| Percussionaire Corp. | Sandpoint, ID, United States | Manufacturer | 1 | April 18, 1991 | 0 | 2 | 1 | api.fda.gov |
| Respironics Inc. | Murrysville, PA, United States | Complaint file establishment, Manufacturer | 1 | December 14, 2012 | 0 | 0 | 0 | api.fda.gov |
| Creative Foam Corporation dba MT. OLIVE MFG | Mooresville, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ventec Life Systems, Inc. | Woodinville, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ventec Life Systems, Inc. | Bothell, WA, United States | Complaint file establishment, Manufacturer, Specification developer | 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.