Data / Medical devices / Mexico / Vapotherm-Mexico S de RL de CV
Vapotherm-Mexico S de RL de CV: FDA-registered device maker in Alvaro Obregon Mexico, Mexico, 1 510(k) clearance
Vapotherm-Mexico S de RL de CV is registered with the FDA (registration 3048101987) in Alvaro Obregon Mexico, Mexico. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 17, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3048101987
- Address
- 3ra Cerrada de Minas 501 Local 9 Arvide, Alvaro Obregon Mexico, Mexico, 01280
- Owner or operator
- VAPOTHERM, INC. (9038880)
- Roles
- Exporter to the US
- First device listed
- October 27, 2008
- Registered through
- 2026
- Brand names listed
- PF-ADPC-LOW
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Humidifier, Respiratory Gas, (Direct Patient Interface) | BTT | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| July 17, 2008 | K072845 | PRECISION FLOW | BTT | Substantially Equivalent | Vapotherm, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 17, 2008. 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.