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Sign in to claim this brandResmed Corp
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 9001 Spectrum Center Boulevard, San Diego, CA, 92123
- Website
- resmed.com
- —
- —
- [email protected]
- Phone
- 800-424-0737
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000115734
- DUNS Number
- 080243150
Catalogue (404)
Page 9 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Resmed Meridian Mask | K050142 | FDA 510(k) | Class II | Active |
| AirView | K151901 | FDA 510(k) | Class II | Active |
| Sullivan Mirage Full Face Mask | K982530 | FDA 510(k) | Class II | Active |
| Vpap Adapt | K113801 | FDA 510(k) | Class II | Active |
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FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jul 12, 2016 | Z-2550-2016 | — | terminated | Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask. |
| Jan 13, 2016 | Z-0746-2016 | — | terminated | Resmed Corporation is recalling Astral 100, 150 External Battery because of a start-up issue. |
| Apr 23, 2007 | Z-1006-2007 | — | terminated | S8 devices manufactured between July 2004 and May 15, 2006 are susceptible to fatigue in the connection of the AC appliance inlet connector and the power supply (power cord) leading to possible failure (short circuit, electrical failure, sparks, smoke). |