Data / Medical devices / Stimulator, Hypoglossal Nerve, Implanted, Apnea / United States
FDA-registered makers of Stimulator, Hypoglossal Nerve, Implanted, Apnea in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Stimulator, Hypoglossal Nerve, Implanted, Apnea (product code MNQ). 2 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
- Stimulator, Hypoglossal Nerve, Implanted, Apnea
- Product code
- MNQ
- Country
- United States
Makers of Stimulator, Hypoglossal Nerve, Implanted, Apnea in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Inspire Medical Systems Inc | Golden Valley, MN, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 1 | 4 | 1 | api.fda.gov | |
| Inspire Medical Systems Inc | Golden Valley, MN, United States | Manufacturer, Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Avivomed, Inc | Roseville, MN, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| CDR Manufacturing, Inc., DBA Keytronic | Oakdale, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cirtec Medical | Brooklyn Park, MN, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cirtec Medical | Enfield, CT, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Greatbatch Medical | Minneapolis, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nortech Systems, Inc. | Milaca, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Osypka Medtec Inc. | Longmont, CO, 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.