Data / Medical devices / United States / Invent Medical Corporation
Invent Medical Corporation: FDA-registered device maker in Carlsbad, CA, United States, 1 510(k) clearance
Invent Medical Corporation is registered with the FDA (registration 3016052406) in Carlsbad, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 14, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016052406
- Address
- 2788 Loker Ave W, Carlsbad, CA, United States, 92010
- Owner or operator
- Invent Medical Corporation (10081562)
- Roles
- Manufacturer, Specification developer
- First device listed
- April 24, 2021
- Registered through
- 2026
- Brand names listed
- 15mm Heated Tubing, HFC-GOLD, Hft150
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Nasal, Oxygen | CAT | 1 | Specification developer | accessdata.fda.gov |
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Specification developer | accessdata.fda.gov |
| Humidifier, Respiratory Gas, (Direct Patient Interface) | BTT | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 14, 2024 | K233707 | HFT150 | BTT | Substantially Equivalent | Invent Medical Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Circuit, Breathing (W Connector, Adaptor, Y Piece)
- All makers of Cannula, Nasal, Oxygen
- All makers of Humidifier, Respiratory Gas, (Direct Patient Interface)
Updated June 14, 2024. 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.