7 premarket notifications (510(k)s) from applicants based in New Hampshire were decided by FDA in the last 12 months, newest first. Each row links to FDA's own record.
| Decided | Applicant | Device | Area | Where | Record |
|---|---|---|---|---|---|
| 2026-10-02 | Argus Cognitive, Inc. | Neurora QPF | Neurology | Hanover, New Hampshire | K260064 |
| 2026-09-09 | Argus Cognitive, Inc. | ReVISION 2 QIH | Radiology | Hanover, New Hampshire | K251417 |
| 2026-07-24 | Deka R&D Corp | RemunityPRO+ Pump for Remodulin® (treprostinil) Injection FRN | General Hospital | Manchester, New Hampshire | K253703 |
| 2026-06-17 | Deka Research and Development | twiist Automated Insulin Delivery (AID) System QFG | Clinical Chemistry | Manchester, New Hampshire | K261672 |
| 2026-06-03 | Deka Research and Development | iiSure Infusion Set FPA | General Hospital | Manchester, New Hampshire | K261530 |
| 2026-04-13 | Vapotherm, Inc. | HVT 2.0 BTT | Anesthesiology | Exeter, New Hampshire | K254078 |
| 2026-01-15 | Sleepnet Corporation | Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask BZD | Anesthesiology | Hampton, New Hampshire | K251847 |
Where this comes from
Before most medical devices can be sold in the United States, the maker submits a premarket notification, a 510(k), and FDA decides whether the device is substantially equivalent to one already on the market. Every row here is one of those decisions, linked to FDA's own record of it. The product area is the medical specialty FDA files the device under; the location is the applicant's, as the submission gives it.
A clearance means the agency found the device substantially equivalent; it is not an endorsement. Where an applicant also files with the SEC under the same name in the same state, it links to that company's page.
Cite this page
https://mentionfox.com/fda/510k/state/nh